Carbendazim flow

Hauptinformation

  • Handelsname:
  • Carbendazim flow
  • 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:
  • Carbendazim flow
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Saatbeizmittel Fungizid

Weitere Informationen

Status

  • Quelle:
  • UFAG - Ufficio federale dell'agricoltura. OFAG - Office fédéral de l'agriculture. BLW - Bundesamt für Landwirtschaft.
  • Zulassungsnummer:
  • W-5241
  • Letzte Änderung:
  • 06-09-2017

Packungsbeilage

Produkt:

Handelsbezeichnung: Carbendazim flow

Bewilligung beendet: Ausverkaufsfrist: 30.04.2017, Aufbrauchfrist: 30.04.2018

Produktekategorie

Bewilligungsinhaber Eidg. Zulassungsnummer

Saatbeizmittel

Fungizid

Omya (Schweiz) AG W-5241

Stoff(e)

Gehalt

Formulierungscode

Wirkstoff:

Carbendazim

44.8 % 510 g/l

SL Wasserlösliches Konzentrat

Anwendungen

A Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

O allg.

Blüten- und Zweigdürre

Konzentration: 0.1 %

Aufwandmenge: 1.6 l/ha

Anwendung: Während der Blüte.

1, 2, 3, 4

O Apfel

Kelchfäule (Botrytis cinerea)

Konzentration: 0.1 %

Aufwandmenge: 1.6 l/ha

Anwendung: Während der Blüte.

3, 4

gedeckte Kulturen:

Gurken

Schwarze Wurzelfäule der Gurke

Aufwandmenge: 1 g/Pflanze

Anwendung: 2-3 x giessen, bis

spätestens vor Erntebeginn.

G Knollensellerie

Septoria-Blattfleckenkrankheit des

Selleries

Konzentration: 0.09 %

Wartefrist: 3 Woche(n)

gedeckte Kulturen:

Tomaten

Samtfleckenkrankheit der Tomate

Konzentration: 0.09 %

Wartefrist: 3 Tage

F Pflanzkartoffeln

Rhizoctonia-solani-Krankheit

Anwendung: 360 ml/100 lt Wasser,

3 Minuten tauchen.

Z allg.

Blattfleckenpilze

Konzentration: 0.06 - 0.12 %

Anwendung: Spritzen.

A Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

Z allg.

Krankheiten durch pathogene

Bodenpilze

Konzentration: 0.6 %

Anwendung: Giessen.

Z Blautanne

Knospensterben der Blautanne

Konzentration: 0.06 - 0.12 %

Anwendung: Spritzen.

Z Primeln

Ramularia-Blattfleckenkrankheit an

Primeln

Konzentration: 0.06 - 0.12 %

Anwendung: Spritzen.

Z Wacholder

Zweigsterben an Wacholder

Konzentration: 0.06 - 0.12 %

Anwendung: Spritzen.

Auflagen und Bemerkungen:

Bei Kirschen bis Schorniggelstadium (I-J).

2 Luftapplikationen pro Jahr.

Die angegebene Aufwandmenge bezieht sich auf ein Baumvolumen von 10'000 m³ pro ha.

Maximal 2 Behandlungen pro Jahr.

Die Säcke müssen die Aufschrift 'Gebeiztes Pflanzgut' tragen.

Gefahrenkennzeichnungen:

R 46 Kann vererbbare Schäden verursachen.

R 50/53 Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen

haben.

R 60 Kann die Fortpflanzungsfähigkeit beeinträchtigen.

R 61 Kann das Kind im Mutterleib schädigen.

S 01 Unter Verschluss aufbewahren.

S 02 Darf nicht in die Hände von Kindern gelangen.

S 45 Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).

S 53 Exposition vermeiden - vor Gebrauch besondere Anweisungen einholen.

S 57 Zur Vermeidung einer Kontamination der Umwelt geeigneten Behälter verwenden.

S 60 Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.

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

Gefahrensymbole und -bezeichnungen:

Kurzkennzeichnung

Symbol

Gefahrenbezeichnung Umweltgefährlich Giftig

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.

9-10-2018

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Peer review of the pesticide risk assessment for the active substance flumioxazin in light of negligible exposure data submitted

Published on: Mon, 08 Oct 2018 00:00:00 +0200 The conclusions of EFSA following the peer review of the initial risk assessment carried out by the competent authority of the rapporteur Member State, Czech Republic, for the pesticide active substance flumioxazin are reported. The European Commission requested EFSA to conduct a peer review and provide its conclusions on whether exposure of humans to flumioxazin can be considered negligible, taking into account the European Commission's draft guidance on th...

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22-9-2018

Risk assessment of new sequencing information on genetically modified carnation FLO‐40689‐6

Risk assessment of new sequencing information on genetically modified carnation FLO‐40689‐6

Published on: Fri, 21 Sep 2018 00:00:00 +0200 The GMO Panel has previously assessed genetically modified (GM) carnation FLO‐40689‐6 and concluded that there is no scientific reason to consider that the import, distribution and retailing in the EU of carnation FLO‐40689‐6 cut flowers for ornamental use will cause any adverse effects on human health or the environment. On 27 October 2017, the European Commission requested EFSA to analyse new nucleic acid sequencing data and updated bioinformatics data for...

Europe - EFSA - European Food Safety Authority Publications

12-9-2018

Application of data science in risk assessment and early warning

Application of data science in risk assessment and early warning

Published on: Mon, 27 Aug 2018 00:00:00 +0200 The currently applied approaches, procedures and tools used for the identification of emerging risks vary greatly among Member States of the EU. EFSA established a structured approach for emerging risk identification that mainly consists of systematically searching, collecting, collating and analysing information and data. In addition, EFSA concluded that new methodologies and tools are needed to facilitate efficient and transparent sharing of data, knowledg...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Scientific Opinion about the Guidance of the Chemical Regulation Directorate (UK) on how aged sorption studies for pesticides should be conducted, analysed and used in regulatory assessments

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Published on: Mon, 27 Aug 2018 00:00:00 +0200 The EFSA Panel on Plant Protection Products and their Residues reviewed the guidance on how aged sorption studies for pesticides should be conducted, analysed and used in regulatory assessment. The inclusion of aged sorption is a higher tier in the groundwater leaching assessment. The Panel based its review on a test with three substances taken from a data set provided by the European Crop Protection Association. Particular points of attention were the quali...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Modification of the existing maximum residue levels for prohexadione in various oilseeds

Modification of the existing maximum residue levels for prohexadione in various oilseeds

Published on: Mon, 27 Aug 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant BASF SE submitted a request to the competent national authority in France to modify the existing maximum residue levels (MRL) for the active substance prohexadione in linseeds, poppy seeds, sunflower seeds, rape seeds, mustard seeds and gold of pleasure seeds. The data submitted in support of the request were found to be sufficient to derive MRL proposals for all oilseeds under consid...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Safety assessment of the process ‘General Plastic’, based on Starlinger Decon technology, used to recycle post‐consumer PET into food contact materials

Safety assessment of the process ‘General Plastic’, based on Starlinger Decon technology, used to recycle post‐consumer PET into food contact materials

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Europe - EFSA - European Food Safety Authority Publications

7-8-2018

Voluntary Recall Notice of El Guapo Jamaica Hibiscus Flower Pouches Due to Unlabeled Peanut Allergen

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Mojave Foods Corporation is initiating a voluntary recall of four sizes of El Guapo Jamaica Hibiscus Flower packages in flexible packaging due to an unlabeled peanut allergen

FDA - U.S. Food and Drug Administration

24-7-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on voluntary recalls of Ritz, Goldfish and other products issued out of an abundance of caution

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The U.S. Food and Drug Administration is working with Mondelēz International, Inc., Pepperidge Farm Inc. and Flowers Foods, Inc. to initiate voluntarily recalls of certain products due to a potential risk that one of the ingredients may have been contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

23-7-2018

Flowers Foods Issues Voluntary Recall on Mrs. Freshley’s and Other Brands of Swiss Rolls and Captain John Derst’s Old Fashioned Bread

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FDA - U.S. Food and Drug Administration

2-7-2018

May Flower International Inc. Issues a Allergy Alert on Undeclared Milk Allergens in “3+2 Soda Crackers”

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May Flower International Inc. of 5672 49th Place, Maspeth, NY, is recalling its 4.4 ounce packages of “3+2 Soda Crackers” because they may contain undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life threatening allergic reactions if they consume this product.

FDA - U.S. Food and Drug Administration

26-6-2018

Huish Outdoors recalls Oceanic and Hollis Scuba Diving Regulators

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Health Canada

23-6-2018

Dringende Sicherheitsinformation zu Mentype® MycoDermQS Lateral Flow von Biotype Diagnostic GmbH

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Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

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

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FDA - U.S. Food and Drug Administration

5-6-2018

Dringende Sicherheitsinformation zu Biograph mCT systems, Biograph mCT Flow systems von Siemens Medical Solutions USA, Inc. Molecular Imaging

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

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

31-5-2018

Abbott Implements Corrective Action for Heartmate 3 Heart Pump

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FDA - U.S. Food and Drug Administration

25-5-2018

Urgent Medical Device Recall: Sam XT Extremity Tourniquet

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FDA - U.S. Food and Drug Administration

22-5-2018

HeartMate 3™ Left Ventricular Assist System: Class I Recall - Due to Potential Malfunction that may Lead to Graft Occlusion

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FDA - U.S. Food and Drug Administration

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