Soft Unkrautvertilger

Informazioni principali

  • Nome commerciale:
  • Soft Unkrautvertilger
  • Utilizzare per:
  • Piante
  • Tipo di medicina:
  • Agrochimico

Documenti

  • per i professionisti:
  • Il foglio illustrativo per questo prodotto non è al momento disponibile, é possibile inviare una richiesta al nostro Servizio Clienti ed essere avvisati nel momento in cui è disponibile sulla nostra piattaforma.


    Richiedi il foglio illustrativo per i professionisti.

Localizzazione

  • Disponibile in:
  • Soft Unkrautvertilger
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Erbicida

Altre informazioni

Status

  • Fonte:
  • UFAG - Ufficio federale dell'agricoltura. OFAG - Office fédéral de l'agriculture. BLW - Bundesamt für Landwirtschaft.
  • Numero dell'autorizzazione:
  • W-4835
  • Ultimo aggiornamento:
  • 06-09-2017

Foglio illustrativo: composizione, posologia, indicazioni, interazioni, gravidanza, allattamento, effetti indesiderati, controindicazioni

Prodotto:

Denominazione commerciale: Soft Unkrautvertilger

Autorizzazione revocata: Termine per la svendita: 31.05.2017, Termine per l'utilizzo: 31.05.2018

Categoria di

prodotti

Titolare dell'autorizzazione

Numero federale di

omologazione

Erbicida

Sintagro AG

W-4835

Principio

Tenore

Codice di

formulazione

Principio

attivo:

Glifosato

0.96 % 9.71 g/l

[Pari a 1.30% di Glifosato - isopropile sale di ammonio (13.1

g/l)]

AL liquido (utilizzo

senza diluizione)

Applicazioni

A Coltura

Agente

patogeno/Efficacia

Dosaggio

Restrizioni

B Mora

Dicotiledoni annuali

(malerbe)

Gramigna

Monocotiledoni annuali

(malerbe).

Dose: 20

ml/m²

1, 2, 3, 4

B Mora

Dicotiledoni pluriennali

(malerbe)

Monocotiledoni perenni

(malerbe)

Dose: 40

ml/m²

1, 2, 3, 4

Frutta a granelli

Frutta a nocciolo

Dicotiledoni annuali

(malerbe)

Gramigna

Monocotiledoni annuali

(malerbe).

Dose: 20

ml/m²

1, 2, 3, 4

O Frutta a granelli

Frutta a nocciolo

Dicotiledoni pluriennali

(malerbe)

Monocotiledoni perenni

Dose: 40

ml/m²

1, 2, 3, 4

A Coltura

Agente

patogeno/Efficacia

Dosaggio

Restrizioni

(malerbe)

Arbusti

Boschetti (al di fuori del bosco)

Dicotiledoni annuali

(malerbe)

Gramigna

Monocotiledoni annuali

(malerbe).

Dose: 20

ml/m²

1, 2, 3, 4

Arbusti

Boschetti (al di fuori del bosco)

Dicotiledoni pluriennali

(malerbe)

Monocotiledoni perenni

(malerbe)

Dose: 40

ml/m²

1, 2, 3, 4

Z Piante ornamentali annuali e biennali

Dicotiledoni annuali

(malerbe)

Gramigna

Monocotiledoni annuali

(malerbe).

Dose: 20

ml/m²

1, 2, 3, 5

Z Piante ornamentali annuali e biennali

Dicotiledoni pluriennali

(malerbe)

Monocotiledoni perenni

(malerbe)

Dose: 40

ml/m²

1, 2, 3, 5

Z Tappeti erbosi e terreni sportivi

Dicotiledoni annuali

(malerbe)

Gramigna

Monocotiledoni annuali

(malerbe).

Dose: 20

ml/m²

1, 2, 3

Z Tappeti erbosi e terreni sportivi

Dicotiledoni pluriennali

(malerbe)

Monocotiledoni perenni

(malerbe)

Dose: 40

ml/m²

1, 2, 3

Scarpate e strisce verdi lungo le vie di

comunicazione (conformemente ORRPChim)

Dicotiledoni annuali

(malerbe)

Gramigna

Monocotiledoni annuali

(malerbe).

Dose: 20

ml/m²

1, 2, 3, 6

Scarpate e strisce verdi lungo le vie di

comunicazione (conformemente ORRPChim)

Dicotiledoni pluriennali

(malerbe)

Monocotiledoni perenni

(malerbe)

Dose: 40

ml/m²

1, 2, 3, 6

Restrizioni e osservazioni:

L'utente deve essere accuratamente informato sui rischi di danni. Occorre indicare le possibilità di

prevenzione.

Non devono esserci precipitazioni durante almeno 6 ore dopo il trattamento.

Per il trattamento di focolai di malerbe/pianta per pianta, la concentrazione della poltiglia per

irrorazione è indicata in funzione delle specie di malerbe.

Trattamento al più tardi entro fine agosto. Non possono essere trattate le parti vegetali verdi e le

vigne con sistemi di potatura corta (gobelet, cordoni permanenti, eccetera).

Trattamento al più tardi fino a 2 settimane prima della semina o della piantagione.

Conformemente all'ordinanza sulla riduzione dei rischi inerenti ai prodotti chimici (ORRPChim,

allegato 2.5), soltanto trattamenti pianta per pianta su piante problematiche su scarpate e strisce

verdi lungo le strade e i binari ferroviari, sempre che non possono essere combattute con altre

misure.

Caratterizzazione di pericolo:

Per evitare rischi per l'uomo e per l'ambiente seguire le istruzioni per l'uso.

S 02 Conservare fuori della portata dei bambini.

SP 1 Non contaminare l'acqua con il prodotto o il suo imballaggio.

In caso di dubbio valgono soltanto i documenti originali dell'omologazione. La menzione di un prodotto,

principio attivo o di una ditta non rappresenta alcuna raccomandazione.

16-1-2019

Software for Benchmark Dose Modelling

Software for Benchmark Dose Modelling

Published on: Mon, 14 Jan 2019 In specific contract No 7 issued under the framework agreement OC/EFSA/AMU/2015/02, EFSA requested Open Analytics to extend the Web application for Benchmark Dose Modelling built under specific contracts No 3 and No 4. The Web application is further developed in R with focus on creating a graphical module to evaluate model fit and to modify specific plot settings, as specified in the Technical Annex to Specific Contract No 7. The web application includes the latest develop...

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Dollarama recalls MONTOY Little Princess Doll

Dollarama recalls MONTOY Little Princess Doll

The plastic doll contains levels of phthalates that exceed the allowable limit and may pose a chemical hazard. Studies suggest that certain phthalates, including DEHP, may cause reproductive and developmental abnormalities in young children when soft vinyl products containing phthalates are sucked or chewed for extended periods.

Health Canada

19-12-2018

The Manhattan Toy Company recalls "Find the Bear" Soft Books

The Manhattan Toy Company recalls "Find the Bear" Soft Books

A metal grommet used to attach a fabric flap to a page in the book may pull apart posing a small parts choking hazard for small children.

Health Canada

19-12-2018

Medtronic Announces Worldwide Voluntary Field Corrective Action; Company Issues Software Update for Puritan Bennett™ 980 (Pb980) Ventilator Series

Medtronic Announces Worldwide Voluntary Field Corrective Action; Company Issues Software Update for Puritan Bennett™ 980 (Pb980) Ventilator Series

Medtronic (NYSE:MDT) is notifying customers worldwide of a voluntary field corrective action for its Puritan Bennett™ 980 (PB980) ventilator series. Medtronic initiated this field action on September 19, 2018.

FDA - U.S. Food and Drug Administration

4-12-2018

Joint project on Benchmark Dose modelling with RIVM

Joint project on Benchmark Dose modelling with RIVM

Published on: Mon, 03 Dec 2018 A web application for PROAST, a software package for BMD modelling, was developed to make the use of the BMD approach significantly easier for toxicologists and risk assessors. In addition, model averaging was included in the software, for the most frequently occurring types of data in toxicological studies. The PROAST web application now allows for applying model averaging for the case of both quantal and continuous data, as well as for combined datasets (dose‐response da...

Europe - EFSA - European Food Safety Authority Publications

1-12-2018

Safety assessment of the process ‘RecyPET Hungária’, based on RecyPET Hungária technology, used to recycle post‐consumer PET into food contact materials

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Published on: Fri, 30 Nov 2018 The EFSA Panel on Food Contact Materials, Enzymes and Processing Aids (CEP) assessed the safety of the recycling process RecyPET Hungária (EU register number RECYC0146). The input is hot caustic washed and dried poly(ethylene terephthalate) (PET) flakes originating from collected post‐consumer PET containers, containing no more than 5% of PET from non‐food applications. The flakes are dried and extruded. The output of the extrusion step is cut into pellets in an underwater...

Europe - EFSA - European Food Safety Authority Publications

27-11-2018

INNUENDO: A cross‐sectoral platform for the integration of genomics in the surveillance of food‐borne pathogens

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Published on: Mon, 26 Nov 2018 Abstract In response to the EFSA call New approaches in identifying and characterizing microbial and chemical hazards, the project INNUENDO (https://sites.google.com/site/theinnuendoproject/) aimed to design an analytical platform and standard procedures for the use of whole‐genome sequencing in surveillance and outbreak investigation of food‐borne pathogens. The project firstly attempted to identify existing flaws and needs, and then to provide applicable cross‐sectorial ...

Europe - EFSA - European Food Safety Authority Publications

23-11-2018

FDA Classifies Field Action Related to Fc 500™ And Epics® As Class 1 Recall Beckman Coulter Life Sciences Committed to Helping Customers Take Prompt, Appropriate Actions

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Beckman Coulter Life Sciences today announced the previously communicated global voluntary recall launched in January 2018 related to the FC 500™ Series Flow Cytometers (FC 500), COULTER® EPICS® XL™ and COULTER® EPICS® XL-MCL™ Flow Cytometer with System II Software (together referred to as the EPICS) has been classified as Class 1 by the U.S. Food and Drug Administration (FDA).

FDA - U.S. Food and Drug Administration

19-11-2018

Dollarama recalls MONTOY Doll and Toy Furniture Set

Dollarama recalls MONTOY Doll and Toy Furniture Set

The plastic doll and furniture toy set contains levels of phthalates that exceed the allowable limit and may pose a chemical hazard. Studies suggest that certain phthalates, including DEHP, may cause reproductive and developmental abnormalities in young children when soft vinyl products containing phthalates are sucked or chewed for extended periods.

Health Canada

10-11-2018

Pest categorisation of Popillia japonica

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Published on: Thu, 08 Nov 2018 00:00:00 +0100 The Panel on Plant Health performed a pest categorisation of Popillia japonica(Coleoptera: Scarabaeidae) for the EU. P. japonica is a distinguishable species listed in Annex IAII of Council Directive 2000/29/EC. It is native to Japan but established in the USA in the early 20th century. It spreads from New Jersey to most US states east of the Mississippi, some to the west and north into Canada. P. japonica feeds on over 700 plant species. Adults attack folia...

Europe - EFSA - European Food Safety Authority Publications

1-11-2018

Pest categorisation of Conotrachelus nenuphar

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Published on: Wed, 31 Oct 2018 00:00:00 +0100 The EFSA Panel on Plant Health performed a pest categorisation of Conotrachelus nenuphar (Herbst) (Coleoptera: Curculionidae), for the EU. C. nenuphar is a well‐defined species, recognised as a serious pest of stone and pome fruit in the USA and Canada where it also feeds on a range of other hosts including soft fruit (e.g. Ribes,Fragaria) and wild plants (e.g. Crataegus). Adults, which are not good flyers, feed on tender twigs, flower buds and leaves. Femal...

Europe - EFSA - European Food Safety Authority Publications

21-9-2018

Scientific guideline:  Guideline on determination of withdrawal periods for edible tissues - Revision 1, adopted

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Europe - EFSA - European Food Safety Authority EFSA Journal

12-9-2018

Application of data science in risk assessment and early warning

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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

11-9-2018

Update of the Xylella spp. host plant database

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Europe - EFSA - European Food Safety Authority Publications

11-9-2018

Livestock Health and Food Chain Risk Assessment

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Europe - EFSA - European Food Safety Authority Publications

30-8-2018

Grant agreement for piloting the Framework Partnership Agreement between the National data provider organisations in Cyprus and EFSA – Final report

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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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Europe - EFSA - European Food Safety Authority Publications

7-8-2018

Dollarama recalls the Skip Ball toy

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Health Canada

10-7-2018

Ortovox Canada recalls Ortovox 3 Avalanche Transceivers

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Health Canada

29-5-2018

Allergan Issues Nationwide Voluntary Recall of TAYTULLA® Softgel Capsules 1mg/20mcg Sample Packs Due to Out of Sequence Capsules

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FDA - U.S. Food and Drug Administration

25-5-2018

Link Product Solutions Limited recalls Summer Time TM Puffer Balls

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These toys do not meet the Canadian safety requirements for toys. Some of the soft, stretchy parts of the toys can stretch to extreme lengths, posing a strangulation hazard to children.

Health Canada

11-12-2018

Regulation of Software as a Medical Device

Regulation of Software as a Medical Device

Updated information on the regulation of Software as a Medical Device

Therapeutic Goods Administration - Australia

30-11-2018

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall:  https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

.@US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevicepic.twitter.com/YU9Iq

. @US_FDA issues class I recall, the most serious type pf recall: Synaptive Medical Recalls BrightMatter Guide with SurfaceTrace Registration Due to Software Defect. Read more about the recall: https://go.usa.gov/xPMEn  #MedicalDevice pic.twitter.com/YU9Iq3Yw0b

FDA - U.S. Food and Drug Administration

19-11-2018

By providing more clarity around how these prescription-drug-use-related software products will be regulated, #FDA hopes to promote development of these innovations. We believe these innovative products can help significantly improve patients’ health

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FDA - U.S. Food and Drug Administration

24-9-2018

Tomorrow, September 25th at 9:15 AM, join the #FDA for a session at #MedTechCon about our #DigitalHealth Software Precertification #FDAPrecert Pilot Program...

Tomorrow, September 25th at 9:15 AM, join the #FDA for a session at #MedTechCon about our #DigitalHealth Software Precertification #FDAPrecert Pilot Program...

Tomorrow, September 25th at 9:15 AM, join the #FDA for a session at #MedTechCon about our #DigitalHealth Software Precertification #FDAPrecert Pilot Program...

FDA - U.S. Food and Drug Administration

7-8-2018

Research: Software as a Medical Device and Cyber Security for Medical Devices

Research: Software as a Medical Device and Cyber Security for Medical Devices

Opportunity to participate in CSIRO research to inform new Australian medical device industry guidance

Therapeutic Goods Administration - Australia

18-7-2018

Knowing what software is included in a device means users and manufacturers can better assess and remediate potential cybersecurity threats that may emerge. #FDA looks forward to participating in the SBOM workstream and engaging broader perspective from t

Knowing what software is included in a device means users and manufacturers can better assess and remediate potential cybersecurity threats that may emerge. #FDA looks forward to participating in the SBOM workstream and engaging broader perspective from t

Knowing what software is included in a device means users and manufacturers can better assess and remediate potential cybersecurity threats that may emerge. #FDA looks forward to participating in the SBOM workstream and engaging broader perspective from the community.

FDA - U.S. Food and Drug Administration

18-7-2018

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a me

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a me

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a medical device.

FDA - U.S. Food and Drug Administration

29-5-2018

FDA Open Docket now available for feedback on benefits and risks of software that are not devices-  https://go.usa.gov/xQdfx  #MedicalDevice #21CenturyAct #DigitalHealth

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FDA Open Docket now available for feedback on benefits and risks of software that are not devices- https://go.usa.gov/xQdfx  #MedicalDevice #21CenturyAct #DigitalHealth

FDA - U.S. Food and Drug Administration