STAIN BLASTER MULTI-PURPOSE

المعلومات الرئيسية

  • اسم تجاري:
  • STAIN BLASTER MULTI-PURPOSE
  • 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:
  • STAIN BLASTER MULTI-PURPOSE
    كازاخستان
  • اللغة:
  • العربية

معلومات أخرى

الحالة

  • المصدر:
  • Ecolab
  • تخويل:
  • 915494-01
  • اخر تحديث:
  • 12-03-2018

ملخص خصائص المنتج

STAIN BLASTER MULTI-PURPOSE

915494-01

1 / 8

STAIN BLASTER MULTI-PURPOSE

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 :

21.08.2017

GHS

STAIN BLASTER MULTI-PURPOSE

915494-01

2 / 8

:

:

:

(%)

distillates (petroleum), hydrotreated light

64742-47-8

10 - 30

Propylene glycol

57-55-6

10 - 30

alcohols, c12-16, ethoxylated

68551-12-2

10 - 30

Linear Alkylbenzenesulphonates

27177-77-1

5 - 10

fatty acids, tall-oil, compds. with triethanolamine

68132-46-7

5 - 10

fatty acids, coco, compds. with triethanolamine

61790-64-5

5 - 10

triethanolamine

102-71-6

5 - 10

poly(oxy-1,2-ethanediyl), a-(2-propylheptyl)-w-

hydroxy-

160875-66-1

1 - 5

Linear Alkylbenzenesulphonates

27323-41-7

1 - 5

d-Limonene

5989-27-5

1 - 5

STAIN BLASTER MULTI-PURPOSE

915494-01

3 / 8

0 °C

50 °C

distillates (petroleum),

hydrotreated light

64742-47-8

200 mg/m3

ARE OEL

0.2 mg/m3

ARE OEL

Propylene glycol

57-55-6

TWA OEL-RL

10 mg/m3

TWA OEL-RL

150 ppm

470 mg/m3

triethanolamine

102-71-6

5 mg/m3

BH OEL

STAIN BLASTER MULTI-PURPOSE

915494-01

4 / 8

triethanolamine

102-71-6

5 mg/m3

ARE OEL

7.5 - 8.5

100 %

> 100 °C

0.95 - 1.05

132 mm2/s (40 °C)

STAIN BLASTER MULTI-PURPOSE

915494-01

5 / 8

4,293 mg/kg :

STAIN BLASTER MULTI-PURPOSE

915494-01

6 / 8

Propylene glycol

4 h :

LC50

158.5 mg/l :

alcohols, c12-16, ethoxylated

2,000 mg/kg :

d-Limonene

> 5,000 mg/kg :

96 h :

LC50

5.7 mg/l :

distillates (petroleum), hydrotreated light

48 h :

EC50

> 1,000 mg/l :

Propylene glycol

48 h :

EC50

STAIN BLASTER MULTI-PURPOSE

915494-01

7 / 8

18,340 mg/l :

triethanolamine

48 h :

EC50

609.88 mg/l :

poly(oxy-1,2-ethanediyl), a-(2-propylheptyl)-w-hydroxy-

48 h :

1 mg/l :

distillates (petroleum), hydrotreated light

72 h :

EC50

> 1,000 mg/l :

Propylene glycol

96 h :

EC50

19,000 mg/l :

triethanolamine

72 h :

EC50

> 100 mg/l :

(ADR/ADN/RID)

STAIN BLASTER MULTI-PURPOSE

915494-01

8 / 8

)

(

)

IMDG/

(

21.08.2017

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.



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Joint EFSA and ECDC 2018 workshop on preparedness for a multi‐national food safety/public health incident

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FDA - U.S. Food and Drug Administration

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FDA Investigates Multistate Outbreak of B. cepacia Complex Linked to Medline Remedy Essentials No-Rinse Cleansing Foam (FDA Announcement)

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2-5-2018

Danish-Japanese collaboration on better use of health data

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Danish Medicines Agency

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FDA - U.S. Food and Drug Administration

16-3-2018

"Beyond Yourself Multi Athlete" and unauthorized bulk "Multi-Vitamines" seized from Shop Santé stores in Quebec may pose serious health risks

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Health Canada

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Flawless Beauty, LLC Issues Voluntary Recall of Unapproved Drugs

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FDA - U.S. Food and Drug Administration

5-10-2017

Collection of scientific experience for medicinal cannabis pilot programme

Collection of scientific experience for medicinal cannabis pilot programme

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Danish Medicines Agency

9-7-2013

Voluntary Harmonisation Procedure (VHP) for the assessment of multinational clinical trial applications

Voluntary Harmonisation Procedure (VHP) for the assessment of multinational clinical trial applications

The Voluntary Harmonisation Procedure is a procedure which makes it possible to obtain a coordinated assessment of an application for a clinical trial that is to take place in several European countries.

Danish Medicines Agency

27-6-2011

Danish Pharmacovigilance Update, 16 June 2011

Danish Pharmacovigilance Update, 16 June 2011

Among the articles in this issue of Danish Pharmacovigilance Update, you can read about the removal of contraindication for Velcade® (bortezomib) used for the treatment of multiple myeloma.

Danish Medicines Agency

25-9-2018

Single use devices should not be reused. Your health care provider or emergency personnel may be able to assist you in obtaining a supply of single use devices during an emergency. Click the link to find out how to safely reuse multiple use devices:  http

Single use devices should not be reused. Your health care provider or emergency personnel may be able to assist you in obtaining a supply of single use devices during an emergency. Click the link to find out how to safely reuse multiple use devices: http

Single use devices should not be reused. Your health care provider or emergency personnel may be able to assist you in obtaining a supply of single use devices during an emergency. Click the link to find out how to safely reuse multiple use devices: https://go.usa.gov/xPjCj  pic.twitter.com/yVSNlc5Qb0

FDA - U.S. Food and Drug Administration

22-8-2018

BTVPUR (Merial)

BTVPUR (Merial)

BTVPUR (Active substance: Bluetongue virus vaccine (inactivated) (multistrain: 1-2 strains out of a set of 4)) - Centralised - 2-Monthly update - Commission Decision (2018)5630 of Wed, 22 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/2231/II/10

Europe -DG Health and Food Safety

6-8-2018

Scientific guideline:  Draft guideline on the use of minimal residual disease as a clinical endpoint in multiple myeloma studies, draft: consultation open

Scientific guideline: Draft guideline on the use of minimal residual disease as a clinical endpoint in multiple myeloma studies, draft: consultation open

The guideline aims to address the use of undetectable minimal residual disease (MRD) as an intermediate efficacy endpoint in controlled randomised clinical studies in patients with multiple myeloma (MM), adequately designed to demonstrate efficacy by relevant hard endpoints. MRD as an endpoint in this context would allow earlier approval of new drugs pending final confirmatory data.

Europe - EMA - European Medicines Agency

6-8-2018

Scientific guideline:  ICH M9 on biopharmaceutics classification system based biowaivers - Step 2b - First version, draft: consultation open

Scientific guideline: ICH M9 on biopharmaceutics classification system based biowaivers - Step 2b - First version, draft: consultation open

This new multidisciplinary guideline is proposed to address biopharmaceutics classification system (BCS)-based biowaivers. BCS-based biowaivers may be applicable to BCS Class I and III drugs, however BCS-based biowaivers for these two classes are not recognized worldwide. This means that pharmaceutical companies have to follow different approaches in the different regions. This guideline will provide recommendations to support the biopharmaceutics classification of medicinal products and will provide rec...

Europe - EMA - European Medicines Agency

19-7-2018

Regulatory and procedural guideline:  Qualification opinion on dopamine transporter imaging as an enrichment biomarker for Parkinson’s disease clinical trials in patients with early Parkinsonian symptoms, adopted

Regulatory and procedural guideline: Qualification opinion on dopamine transporter imaging as an enrichment biomarker for Parkinson’s disease clinical trials in patients with early Parkinsonian symptoms, adopted

Critical Path Global Ltd.’s Critical Path for Parkinson’s (CPP) is a multinational consortium of the Critical Path Institute supported by Parkinson’s UK and industry. This broad collaboration of pharmaceutical companies, government agencies, academic institutions, and charities aims to accelerate the development of therapies for Parkinson’s disease (PD).

Europe - EMA - European Medicines Agency

3-7-2018

The Pediatric Medical Device Development public meeting is August 13-14 at #FDA White Oak Campus. Do you know how the FDA defines “pediatrics” for medical device purposes? Click the link for the answer and more info on #Pediatric #MedicalDevices  https://

The Pediatric Medical Device Development public meeting is August 13-14 at #FDA White Oak Campus. Do you know how the FDA defines “pediatrics” for medical device purposes? Click the link for the answer and more info on #Pediatric #MedicalDevices https://

The Pediatric Medical Device Development public meeting is August 13-14 at #FDA White Oak Campus. Do you know how the FDA defines “pediatrics” for medical device purposes? Click the link for the answer and more info on #Pediatric #MedicalDevices https://go.usa.gov/xU2e8 

FDA - U.S. Food and Drug Administration

25-5-2018

Therapeutic Goods (Medicines-Listing) Approval of Application Forms and Specification of Office to which Application Must be Delivered

Therapeutic Goods (Medicines-Listing) Approval of Application Forms and Specification of Office to which Application Must be Delivered

I, Larry Kelly, Acting Deputy Secretary, Health Products Regulation Group, a delegate of the Secretary of the Department of Health for the purposes of section 23C of the Therapeutic Goods Act 1989, make the following instrument under paragraphs 23C(2)(a...

Therapeutic Goods Administration - Australia