ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

المعلومات الرئيسية

  • اسم تجاري:
  • ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT
  • يسخدم من اجل:
  • البشر
  • نوع الدواء:
  • الجهاز الطبي

المستندات

  • لعامة الناس:
  • النشرة المعلومات عن هذا المنتج غير متوفر حاليا، يمكنك إرسال طلب لخدمة العملاء لدينا، ونحن سوف يخطر لك في أقرب وقت ونحن قادرون على الحصول عليه.


    طلب نشرة المعلومات لعامة الناس.

الأقلمة

  • متاح في:
  • ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT
    كازاخستان
  • اللغة:
  • العربية

معلومات أخرى

الحالة

  • المصدر:
  • Ecolab
  • تخويل:
  • 913510
  • اخر تحديث:
  • 12-03-2018

ملخص خصائص المنتج

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

1 / 9

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

0.58 % - 0.78 %

00971 4 8014444

00971 48146800 00971 4 8014000

0020 2 25 37 1195

00212 22 58 25 30 - 35

00971 4 8014444 :

00971 48146800 00971 4 8014000

0020 2 25 37 1195 :

00212 22 58 25 30 - 35 :

09.08.2017

GHS

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

2 / 9

:

:

:

:

:

(%)

Lactic acid

79-33-4

10 - 30

Sodium bisulfate

7681-38-1

5 - 10

25155-30-0

1 - 5

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

3 / 9

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

4 / 9

0 °C

50 °C

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

5 / 9

0.5 - 1.0

100 %

2.1 - 3.2

> 100 °C

1.069 - 1.135

907.757 mm2/s (40 °C)

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

6 / 9

> 5,000 mg/kg :

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

7 / 9

4 h :

> 2 mg/l :

5,000 mg/kg :

Lactic acid

96 h :

LC50

130 mg/l :

Sodium bisulfate

96 h :

LC50

7,960 mg/l :

96 h :

LC50

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

8 / 9

3.2 mg/l :

(ADR/ADN/RID)

)

(

)

ANTIMICROBIAL FRUIT & VEGETABLE TREATMENT

913510

9 / 9

IMDG/

(

09.08.2017

Regulatory Affairs

  • النشرة المعلومات عن هذا المنتج غير متوفر حاليا، يمكنك إرسال طلب لخدمة العملاء لدينا، ونحن سوف يخطر لك في أقرب وقت ونحن قادرون على الحصول عليه.

    طلب نشرة المعلومات لعامة الناس.



  • وثائق في اللغات الأخرى المتاحة هنا

20-7-2018

FDA approves first targeted treatment for patients with relapsed or refractory acute myeloid leukemia who have a certain genetic mutation

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FDA approves new drug for the treatment of adults with acute myeloid leukemia who have a specific genetic mutation and a companion diagnostic to detect specific mutations in the IDH1 gene in patients with AML

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18-7-2018

Orphan designation:  Gevokizumab,  for the: Treatment of Schnitzler syndrome

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18-7-2018

Orphan designation:  Recombinant humanised anti-human interleukin-1 beta monoclonal antibody,  for the: Treatment of Behçet’s disease

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On 1 October 2010, orphan designation (EU/3/10/796) was granted by the European Commission to XOMA Ireland Ltd, Ireland, for recombinant humanised anti-human interleukin-1 beta monoclonal antibody for the treatment of Behçet’s disease.

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Orphan designation:  Gevokizumab,  for the: Treatment of chronic non-infectious uveitis

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On 12 March 2013, orphan designation (EU/3/13/1111) was granted by the European Commission to Les Laboratoires Servier, France, for gevokizumab for the treatment of chronic non-infectious uveitis.

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18-7-2018

Orphan designation:  Thalidomide,  for the: Treatment of multiple myeloma

Orphan designation: Thalidomide, for the: Treatment of multiple myeloma

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Orphan designation:  Lenvatinib,  for the: Treatment of hepatocellular carcinoma

Orphan designation: Lenvatinib, for the: Treatment of hepatocellular carcinoma

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Orphan designation:  Lenvatinib,  for the: Treatment of papillary thyroid cancer

Orphan designation: Lenvatinib, for the: Treatment of papillary thyroid cancer

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Orphan designation:  Avelumab,  for the: Treatment of gastric cancer

Orphan designation: Avelumab, for the: Treatment of gastric cancer

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18-7-2018

Orphan designation:  Azacitidine,  for the: Treatment of acute myeloid leukaemia

Orphan designation: Azacitidine, for the: Treatment of acute myeloid leukaemia

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13-7-2018

FDA approves the first drug with an indication for treatment of smallpox

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FDA today approved TPOXX (tecovirimat), the first drug with an indication for treatment of smallpox.

FDA - U.S. Food and Drug Administration

13-7-2018

Scientific guideline:  Guideline on good pharmacogenomic practice - First version, adopted

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This guideline provides recommendations for the conduct of genomic studies in relation to medical therapy in order to provide high quality information on the impact of genomic variability on drug response. Primary focus is on the analysis of genomic germline DNA. The analysis of somatic DNA and genomic biomarkers for cancer treatment is not being discussed and might be developed as an Annex or in separate guidance.

Europe - EFSA - European Food Safety Authority EFSA Journal

9-7-2018

Statement by FDA Commissioner Scott Gottlieb, M.D., on balancing access to appropriate treatment for patients with chronic and end-of-life pain with need to take steps to stem misuse and abuse of opioids

Statement by FDA Commissioner Scott Gottlieb, M.D., on balancing access to appropriate treatment for patients with chronic and end-of-life pain with need to take steps to stem misuse and abuse of opioids

FDA Commissioner statement on balancing access to appropriate treatment for patients with chronic and end-of-life pain with need to take steps to stem opioid misuse and abuse.

FDA - U.S. Food and Drug Administration

29-6-2018

Orphan designation:  Rufinamide,  for the: Treatment of Lennox-Gastaut syndrome

Orphan designation: Rufinamide, for the: Treatment of Lennox-Gastaut syndrome

Europe - EMA - European Medicines Agency

28-6-2018

FDA Releases Guidance to Help Animal Drug Sponsors with Antimicrobial Animal Drug Sales and Distribution Reporting Requirements

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FDA is releasing Guidance for Industry #252. This small entity compliance guide is intended to help small businesses comply with the Antimicrobial Animal Drug Sales and Distribution final rule.

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

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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

16-6-2018

FDA Investigates Multistate Outbreak of Cyclospora illnesses linked to Del Monte Vegetable Trays

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The U.S. Food and Drug Administration (FDA) along with the Centers for Disease Control and Prevention (CDC) and state and local officials have been investigating a cluster of cyclosporiasis illnesses associated with recalled Del Monte vegetable trays from Kwik Trip/Kwik Star locations in the United States.

FDA - U.S. Food and Drug Administration

14-6-2018

FDA approves first generic versions of Suboxone sublingual film, which may increase access to treatment for opioid dependence

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: FDA approved the first generic versions of Suboxone (buprenorphine and naloxone) sublingual film (applied under the tongue) for the treatment of opioid dependence.

FDA - U.S. Food and Drug Administration

13-6-2018

Orphan designation:  Ivosidenib,  for the: Treatment of acute myeloid leukaemia

Orphan designation: Ivosidenib, for the: Treatment of acute myeloid leukaemia

Europe - EMA - European Medicines Agency

12-6-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s efforts to foster discovery and development of new tools to fight antimicrobial-resistant infections

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The increase in serious antimicrobial drug resistant infections is a critical public health concern and a growing threat to patients. FDA is taking steps to combat antibiotic-resistant bacteria.

FDA - U.S. Food and Drug Administration

9-6-2018

Caito Foods, LLC Voluntarily Recalls Fresh Cut Melon Products Because of Possible Health Risk

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Caito Foods is voluntarily recalling fresh cut watermelon, honeydew melon, cantaloupe and fresh-cut mixed fruit containing one of these melons, produced at the Caito Foods facility in Indianapolis, because these products have the potential to be contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

8-6-2018

Orphan designation:  Mepolizumab,  for the: Treatment of Churg-Strauss syndrome

Orphan designation: Mepolizumab, for the: Treatment of Churg-Strauss syndrome

On 12 March 2013, orphan designation (EU/3/13/1116) was granted by the European Commission to Glaxo Group Ltd, United Kingdom, for mepolizumab for the treatment of Churg-Strauss syndrome.

Europe - EMA - European Medicines Agency

16-7-2018

If you are misusing an #opioid just to keep from getting sick from #withdrawal symptoms, it’s time to break the cycle of dependence. Read our “Finding Quality Treatment for Substance Use Disorders” for hotline and provider information.  http://bit.ly/2EIJ

If you are misusing an #opioid just to keep from getting sick from #withdrawal symptoms, it’s time to break the cycle of dependence. Read our “Finding Quality Treatment for Substance Use Disorders” for hotline and provider information. http://bit.ly/2EIJ

If you are misusing an #opioid just to keep from getting sick from #withdrawal symptoms, it’s time to break the cycle of dependence. Read our “Finding Quality Treatment for Substance Use Disorders” for hotline and provider information. http://bit.ly/2EIJb9l  #MondayMotivation

FDA - U.S. Food and Drug Administration

9-7-2018

Scientific guideline:  Concept paper on the need to develop a reflection paper on development of medicinal products to prevent and treat acute kidney injury, draft: consultation open

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Europe - EMA - European Medicines Agency

13-6-2018

Scientific guideline:  Concept paper on preparation of a revised guideline on the evaluation of medicinal products indicated for treatment of bacterial infections, draft: consultation open

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This concept paper proposes the development of a single guideline on the clinical evaluation of medicinal products indicated for treatment of bacterial infections. The development of this single guideline is intended to merge, revise and add to the guidance that is currently included in two separate documents as follows: guideline on the evaluation of medicinal products indicated for treatment of bacterial infections (CPMP/EWP/558/95 Rev. 2), adopted in 2011 and in force since 2012 and the addendum ...

Europe - EMA - European Medicines Agency