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Hauptinformation

  • Handelsname:
  • Select
  • Verwenden für:
  • Pflanzen
  • Art der Medizin:
  • Agrochemisch

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Select
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Herbizid

Weitere Informationen

Status

  • Quelle:
  • UFAG - Ufficio federale dell'agricoltura. OFAG - Office fédéral de l'agriculture. BLW - Bundesamt für Landwirtschaft.
  • Zulassungsnummer:
  • W-6010
  • Letzte Änderung:
  • 06-09-2017

Packungsbeilage

Produkt:

Handelsbezeichnung: Select

Produktekategorie

Bewilligungsinhaber Eidg. Zulassungsnummer

Herbizid

Stähler Suisse SA

W-6010

Stoff(e)

Gehalt

Formulierungscode

Wirkstoff: Clethodim

25 % 240 g/l

EC Emulsionskonzentrat

Beistoffe, zusätzlich zu deklarieren: Solvent

Naphtha

Anwendungen

A Kultur

Schaderreger/Wirkung Dosierungshinweise

Auflagen

B Erdbeere

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Anwendung: Vor der Blüte und nach der

Ernte.

1, 2

B Erdbeere

Gemeine Quecke

Aufwandmenge: 1 l/ha

Anwendung: Vor der Blüte und nach der

Ernte.

1, 2

O Kernobst

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

O Kernobst

Gemeine Quecke

Aufwandmenge: 1 l/ha

2, 3

W Reben

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

W Reben

Gemeine Quecke

Aufwandmenge: 1 l/ha

2, 3

G Bohnen

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Anwendung: Nachauflauf.

2, 4

A Kultur

Schaderreger/Wirkung Dosierungshinweise

Auflagen

G Bohnen

Gemeine Quecke

Aufwandmenge: 1 l/ha

Anwendung: Nachauflauf.

2, 4

G Erbsen ohne Hülsen

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

1, 2

Estragon

Lorbeer

Petersilie

Rosmarin

Salbei

Schnittlauch

Thymian

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Wartefrist: 60 Tage

Anwendung: Nach der Pflanzung, im

Nachauflauf, nach dem Wiederaustrieb

oder auf etablierten Kulturen.

2, 5, 6

G Karotten

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Wartefrist: 8 Woche(n)

Anwendung: Nachauflauf.

G Karotten

Gemeine Quecke

Aufwandmenge: 1 l/ha

Wartefrist: 8 Woche(n)

Anwendung: Nachauflauf.

G Kopfkohle

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Wartefrist: 4 Woche(n)

Anwendung: Nachauflauf.

G Kopfkohle

Gemeine Quecke

Aufwandmenge: 1 l/ha

Wartefrist: 4 Woche(n)

Anwendung: Nachauflauf.

G Lauch

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Wartefrist: 4 Woche(n)

Anwendung: Nachauflauf.

G Lauch

Gemeine Quecke

Aufwandmenge: 1 l/ha

Wartefrist: 4 Woche(n)

Anwendung: Nachauflauf.

G Rande

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Wartefrist: 60 Tage

Anwendung: Nach dem Auflaufen.

2, 6, 7

G Rande

Gemeine Quecke

Aufwandmenge: 1 l/ha

Wartefrist: 60 Tage

Anwendung: Nach dem Auflaufen.

2, 6, 7

G Schwarzwurzel

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Anwendung: Im 1- bis 2-Blattstadium

der Kultur.

2, 8

A Kultur

Schaderreger/Wirkung Dosierungshinweise

Auflagen

G Spargel [Ertragsanlagen]

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.75 l/ha

Anwendung: Nach der Stechperiode

(BBCH 12 bis 19).

2, 6, 9,

G Spargel [Junganlagen]

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.75 l/ha

Anwendung: Ab Pflanzjahr (BBCH 12

bis 19).

2, 6, 9,

Tomaten

Zwiebeln

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Wartefrist: 8 Woche(n)

Anwendung: Nachauflauf.

Tomaten

Zwiebeln

Gemeine Quecke

Aufwandmenge: 1 l/ha

Wartefrist: 8 Woche(n)

Anwendung: Nachauflauf.

Eiweisserbse

Raps

Sojabohne

Sonnenblume

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

1, 2

Futter- und Zuckerrüben

Kartoffeln

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Futter- und Zuckerrüben

Kartoffeln

Gemeine Quecke

Aufwandmenge: 1 l/ha

Klee zur Saatgutproduktion

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.75 l/ha

2, 8

Lein

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Lein

Gemeine Quecke

Aufwandmenge: 1 l/ha

Mohn

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

2, 8

Sonnenblume

Gemeine Quecke

Aufwandmenge: 1 l/ha

1, 2

Tabak

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

Anwendung: Unmittelbar nach der

Pflanzung.

1, 2

Bäume und Sträucher

(ausserhalb Forst) [in

Baumschulen]

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 0.5 l/ha

2, 6, 9,

Auflagen und Bemerkungen:

Maximal 1 Behandlung pro Jahr.

Ansetzen der Spritzbrühe: Schutzhandschuhe + Schutzbrille oder Visier tragen.

Der Anwender muss informiert werden, dass sich die Wirkung gegen mehrjährige Ungräser,

insbesondere die Quecke, in der Regel nicht über die Dauer der behandelten Kultur erstreckt.

Letzte Behandlung vor der Blüte.

Maximal 1 Behandlung pro Kultur und Jahr.

Bewilligt als geringfügige Verwendung nach Art. 35 PSMV (minor use).

Maximal 1 Behandlung pro Kultur.

Maximal 1 Behandlung.

Maximal 1 Behandlung pro Parzelle und Jahr.

10.Anwendungstechnik: Unterblattbehandlung.

Gefahrenkennzeichnungen:

Darf nicht in die Hände von Kindern gelangen.

EUH 066 Wiederholter Kontakt kann zu spröder oder rissiger Haut führen.

EUH 401 Zur Vermeidung von Risiken für Mensch und Umwelt die Gebrauchsanleitung

einhalten.

H304 Kann bei Verschlucken und Eindringen in die Atemwege tödlich sein.

H317 Kann allergische Hautreaktionen verursachen.

H319 Verursacht schwere Augenreizung.

H336 Kann Schläfrigkeit und Benommenheit verursachen.

H411 Giftig für Wasserorganismen, mit langfristiger Wirkung.

SP 1 Mittel und/oder dessen Behälter nicht in Gewässer gelangen lassen.

SPe 2 Zum Schutz von Grundwasser nicht in Grundwasserschutzzonen (S2) ausbringen.

Signalwort:

Gefahr

Gefahrensymbole und -bezeichnungen:

Kurzkennzeichnung

GHS07

GHS08

GHS09

Symbol

Gefahrenbezeichnung Vorsicht gefährlich Gesundheitsschädigend Gewässergefährdend

Im Zweifelsfall gelten einzig die Originaldokumente der Zulassung. Die Erwähnung eines Produktes,

Wirkstoffes oder einer Firma stellt keine Empfehlung dar und bedeutet nicht, dass sich das Produkt im

Verkauf befindet.

17-10-2018

Applicability of in silico tools for the prediction of dermal absorption for pesticides

Applicability of in silico tools for the prediction of dermal absorption for pesticides

Published on: Tue, 16 Oct 2018 00:00:00 +0200 Based on the “Human in vitro dermal absorption datasets” published as supporting information to the revised EFSA Guidance on Dermal Absorption, in silico models for prediction of absorption across the skin have been evaluated. For this evaluation, a systematic literature search and review was performed, identifying 288 publications describing mathematical models for prediction of dermal absorption. Eleven models potentially relevant to the regulatory assessm...

Europe - EFSA - European Food Safety Authority Publications

11-9-2018

Risk assessment of antimicrobial resistance along the food chain through culture‐independent methodologies

Risk assessment of antimicrobial resistance along the food chain through culture‐independent methodologies

Published on: Mon, 27 Aug 2018 00:00:00 +0200 Antimicrobial resistance (AMR) represents a major challenge for Public Health and the scientific community, and requires immediate and drastic solutions. Acquired resistance to certain antimicrobials is already widespread to such an extent that their efficacy in the treatment of certain life‐threatening infections is already compromised. To date, the emergence and spread of AMR has been attributed to the use, misuse or indiscriminate use of antibiotics as th...

Europe - EFSA - European Food Safety Authority Publications

3-8-2018

HP Hood LLC Recalls Select Units of Half-Gallon Refrigerated Vanilla Almond Breeze Almond Milk due to Possible Milk Allergen

HP Hood LLC Recalls Select Units of Half-Gallon Refrigerated Vanilla Almond Breeze Almond Milk due to Possible Milk Allergen

HP Hood LLC is voluntarily recalling a limited number of half-gallon (1.89 L) cartons of refrigerated Vanilla Almond Breeze almond milk because the product may contain milk, an allergen not listed on the label. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products. The product is safe to consume unless you have a milk allergy or sensitivity. To date, there has been one report of an allergic reaction. Medical ...

FDA - U.S. Food and Drug Administration

31-7-2018

Heat wave: Retailers may refrain from selling non-prescription drugs

Heat wave: Retailers may refrain from selling non-prescription drugs

Due to the summer heat, the Danish Medicines Agency has given Danish retailers dispensation from the requirement to stock a basic selection of medicines if they are having trouble keeping the temperature in their store cool enough for proper storage of the drugs. This dispensation applies until 1 September.

Danish Medicines Agency

17-7-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on new efforts to empower consumers by advancing access to nonprescription drugs

Statement from FDA Commissioner Scott Gottlieb, M.D. on new efforts to empower consumers by advancing access to nonprescription drugs

FDA describes innovative approaches to increase access to a broader selection of nonprescription drug products for consumers

FDA - U.S. Food and Drug Administration

16-7-2018

Utz Quality Foods Issues Allergy Alert on Undeclared Soy in Utz® Carolina Style Barbeque Potato Chips

Utz Quality Foods Issues Allergy Alert on Undeclared Soy in Utz® Carolina Style Barbeque Potato Chips

Utz® Quality Foods, LLC., is voluntarily recalling select expiration dates of Utz® Carolina Style Barbeque Potato Chips due to undeclared soy allergen. This recall was initiated after learning a certain number of packages were mislabeled. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

23-6-2018

Dringende Sicherheitsinformation zu MRSASelect II von Bio-Rad Laboratories France

Dringende Sicherheitsinformation zu MRSASelect II von Bio-Rad Laboratories France

Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

21-6-2018

Now Health Group Inc. Recalls Select Now Real Food® Zesty Sprouting Mix Because of Possible Health Risk

Now Health Group Inc. Recalls Select Now Real Food® Zesty Sprouting Mix Because of Possible Health Risk

NOW Health Group, Inc. (NOW), of Bloomingdale, Illinois, is recalling its NOW Real Food® Zesty Sprouting Mix – Product Code 7271, Lot #3031259 and Lot #3038165 – because its primary ingredient, Crimson Clover Seeds, has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may b...

FDA - U.S. Food and Drug Administration

16-6-2018

Del Monte Fresh Produce N.A., Inc. Voluntarily Recalls Limited Quantity of Vegetable Trays in a Multistate Outbreak of Cyclospora Illnesses in Select Retailers in Illinois, Indiana, Iowa, Michigan, Minnesota, and Wisconsin, Because of Possible Health Risk

Del Monte Fresh Produce N.A., Inc. Voluntarily Recalls Limited Quantity of Vegetable Trays in a Multistate Outbreak of Cyclospora Illnesses in Select Retailers in Illinois, Indiana, Iowa, Michigan, Minnesota, and Wisconsin, Because of Possible Health Risk

Del Monte Fresh Produce N.A., Inc. ("Del Monte Fresh") announced today, the voluntary recall of a limited quantity of 6 oz., 12 oz. and 28 oz. vegetable trays containing fresh broccoli, cauliflower, celery sticks, carrots, and dill dip sold to select retailers in Illinois, Indiana, Iowa, Michigan, Minnesota and Wisconsin. Del Monte was notified by state agencies of the outbreak and its potential involvement.

FDA - U.S. Food and Drug Administration

8-5-2018

Neurovascular Stents Used for Stent-Assisted Coiling (SAC): Letter to Health Care Providers - Recommendations Associated With the Use of These Devices in the Treatment of Unruptured Brain Aneurysms

Neurovascular Stents Used for Stent-Assisted Coiling (SAC): Letter to Health Care Providers - Recommendations Associated With the Use of These Devices in the Treatment of Unruptured Brain Aneurysms

The FDA has received reports associated with the use of these devices in the treatment of unruptured brain aneurysms that suggest some events of peri-procedural stroke and/or death may have been related to procedural risks or patient selection related factors. These factors include patients who had serious co-morbidities resulting in a reduced life expectancy, or who were intolerant to required anticoagulation or anti-platelet therapy.

FDA - U.S. Food and Drug Administration

3-5-2018

Voluntary Recall of Certain Golden Flake, Good Health, UTZ and Weis Brand Tortilla Chips Because of Possible Milk Allergen

Voluntary Recall of Certain Golden Flake, Good Health, UTZ and Weis Brand Tortilla Chips Because of Possible Milk Allergen

Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

27-4-2018

ANSES assesses the efficacy and safety of alternatives to antibiotics in animal husbandry and considers the need for a specific status for these products

ANSES assesses the efficacy and safety of alternatives to antibiotics in animal husbandry and considers the need for a specific status for these products

Today, the Agency is publishing an inventory of alternatives to antibiotics aimed at reducing their use in animal husbandry and based on an original method for evaluating the diverse scientific publications in the field. In its report, ANSES identifies numerous products and substances including compounds, plants, plant extracts and micro-organisms, which are used as alternatives to antibiotics. However, it emphasises the diversity of the data available to assess their safety and efficacy, and their abili...

France - Agence Nationale du Médicament Vétérinaire

25-10-2017

Self-selection of OTC medicines for human use

Self-selection of OTC medicines for human use

On 1 January 2018, new rules on self-selection of OTC medicines become effective. With the change in law, certain OTC medicines will be available for self-selection, which means that they can be sold from shop areas and not only at the counter.

Danish Medicines Agency

8-5-2015

Annual Pharmacovigilance Report 2014

Annual Pharmacovigilance Report 2014

In our annual pharmacovigilance report 2014, you can read about the development in the number of ADR reports, learn about various focus areas and the European collaboration in the pharmacovigilance area as well as see a selection of the ADR signals we processed in 2014, and much more.

Danish Medicines Agency

30-9-2018

Today is the last day to submit applications to the #FDAInnovationChallenge. Thanks to all who have applied.  Selected applications will be announced in November. For more information about the challenge, click the link:   https://go.usa.gov/xP4Nk pic.twi

Today is the last day to submit applications to the #FDAInnovationChallenge. Thanks to all who have applied. Selected applications will be announced in November. For more information about the challenge, click the link: https://go.usa.gov/xP4Nk pic.twi

Today is the last day to submit applications to the #FDAInnovationChallenge. Thanks to all who have applied. Selected applications will be announced in November. For more information about the challenge, click the link: https://go.usa.gov/xP4Nk  pic.twitter.com/pFJZ39oGJC

FDA - U.S. Food and Drug Administration

21-9-2018

Regulatory and procedural guideline:  Draft guideline on the summary of product characteristics (SPC) for veterinary medicinal products containing antimicrobial substances - Revision 1, draft: consultation open

Regulatory and procedural guideline: Draft guideline on the summary of product characteristics (SPC) for veterinary medicinal products containing antimicrobial substances - Revision 1, draft: consultation open

The guideline, which was developed to encourage optimal use and to minimise selection of antimicrobial resistance (AMR), was revised in order to improve consistency of the summary of product characteristics (SPCs) for antimicrobial products in the EU Member States.

Europe - EMA - European Medicines Agency

17-9-2018

The #FDAInnovationChallenge to develop medical devices for #opioid addiction will provide those selected with the opportunity to work directly with the agency to accelerate the development and review of their device proposals to prevent and treat opioid u

The #FDAInnovationChallenge to develop medical devices for #opioid addiction will provide those selected with the opportunity to work directly with the agency to accelerate the development and review of their device proposals to prevent and treat opioid u

The #FDAInnovationChallenge to develop medical devices for #opioid addiction will provide those selected with the opportunity to work directly with the agency to accelerate the development and review of their device proposals to prevent and treat opioid use disorder. #FDA

FDA - U.S. Food and Drug Administration

30-5-2018

The FDA will accept submissions from June 1, 2018, through Sept. 30, 2018, and intends to announce the selected applicants in November 2018.  #FDAInnovationChallenge

The FDA will accept submissions from June 1, 2018, through Sept. 30, 2018, and intends to announce the selected applicants in November 2018. #FDAInnovationChallenge

The FDA will accept submissions from June 1, 2018, through Sept. 30, 2018, and intends to announce the selected applicants in November 2018. #FDAInnovationChallenge

FDA - U.S. Food and Drug Administration

30-5-2018

#FDAInnovationChallenge to develop medical devices for #opioid addiction will provide those selected with the opportunity to work directly with the agency to accelerate the development & review of their device proposals to prevent and treat opioid use dis

#FDAInnovationChallenge to develop medical devices for #opioid addiction will provide those selected with the opportunity to work directly with the agency to accelerate the development & review of their device proposals to prevent and treat opioid use dis

#FDAInnovationChallenge to develop medical devices for #opioid addiction will provide those selected with the opportunity to work directly with the agency to accelerate the development & review of their device proposals to prevent and treat opioid use disorder. #FDA MedicalDevice

FDA - U.S. Food and Drug Administration

16-5-2018

EU/3/12/1034 (Novartis Europharm Limited)

EU/3/12/1034 (Novartis Europharm Limited)

EU/3/12/1034 (Active substance: Humanised monoclonal antibody against P-selectin) - Transfer of orphan designation - Commission Decision (2018)3040 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/026/12/T/02

Europe -DG Health and Food Safety

30-4-2018

Regulatory and procedural guideline:  Draft guideline on the summary of product characteristics (SPC) for veterinary medicinal products containing antimicrobial substances, draft: consultation open

Regulatory and procedural guideline: Draft guideline on the summary of product characteristics (SPC) for veterinary medicinal products containing antimicrobial substances, draft: consultation open

The guideline, which was developed to encourage optimal use and to minimise selection of antimicrobial resistance (AMR), was revised in order to improve consistency of the summary of product characteristics (SPCs) for antimicrobial products in the EU Member States.

Europe - EMA - European Medicines Agency