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Beibei protective clothing

Shanghai Sunland Industrial Co., Ltd is the top manufacturer of Personal Protect Equipment in China, with 20 years’experience. We are the Chinese government appointed manufacturer for government power,personal protection equipment , medical instruments,construction industry, etc. All the products get the CE, ANSI and related Industry Certificates. All our safety helmets use the top-quality raw material without any recycling material.

Why Choose Us
Solutions to meet different needs

We provide exclusive customization of the products logo, using advanced printing technology and technology, not suitable for fading, solid and firm, scratch-proof and anti-smashing, and suitable for various scenes such as construction, mining, warehouse, inspection, etc. Our goal is to satisfy your needs. Demand, do your best.

Highly specialized team and products

Professional team work and production line which can make nice quality in short time..

We trade with an open mind

We abide by the privacy policy and human rights, follow the business order, do our utmost to provide you with a fair and secure trading environment, and look forward to your customers coming to cooperate with us, openly mind and trade with customers, promote common development, and work together for a win-win situation..

24 / 7 guaranteed service

The professional team provides 24 * 7 after-sales service for you, which can help you solve any problems

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Beibei protective clothing
Basics of In-Vitro Diagnostic Medical Device Classification
Basics of In-Vitro Diagnostic Medical Device Classification

For the uninitiated, understanding the basics ,of In-Vitro Diagnostic, Medical Devices can be a confusing process. According to the 1998 medical device directive, IVDD 98/79/EC, an in-,vitro diagnostic, medical device (or IVD) is defined as “any medical device which is a reagent, reagent device, calibrator, control material, ,kit,, instrument, apparatus, equipment or system whether used alone or ...

A guide to the In Vitro Diagnostic Directive
A guide to the In Vitro Diagnostic Directive

A BSI guide to the In ,Vitro Diagnostic, Directive Introduction In ,Vitro Diagnostics, (IVD) is an essential and fast growing part of the global healthcare system, as they add value to patients, medical professionals and the industry along with enhancing the well-being of the population as a whole.

Material Data Safety Sheet MSDS
Material Data Safety Sheet MSDS

IF ON SKIN (or ,hair,): Wash with plenty of soap and water. Take off contaminated ,clothing, and wash before reuse. P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Calssified as Dangerous Goods acording to the criteria of the Australian Code for

Classification of Medical Devices and In Vitro Diagnostic ...
Classification of Medical Devices and In Vitro Diagnostic ...

A total of 350 categories of medical devices and 247 categories ,of in-vitro diagnostic, devices have been classified in accordance with the amended Annexure I as of the 6th of June 2018. Recently, on the 15th of May 2019, further ,classification, of 12 newly notified medical devices have been added to the existing list of classified devices.

Company List Suppliers Distributors Importers ...
Company List Suppliers Distributors Importers ...

Agriculture Apparel & ,Clothing, Automobiles & Motorcycles Beauty & Personal Care Business Services Chemicals, Plastics, and ,Raw Materials, Computer Hardware & Software Construction & Real Estate Consumer Electronics Electrical Equipment & Supplies Energy Products Environment Excess Inventory Fashion Accessories Food & Beverage Furniture & Furnishings General Industrial Equipment Gifts & …

Classification of IVD medical devices
Classification of IVD medical devices

Software as in ,vitro diagnostic, medical devices (IVD s). The highest ,classification, determines the class of IVD Subregulation 3.3 (7) You must consider all of the ,classification, rules to determine the correct class of an IVD. If more than once ,classification, rule applies to your IVD, apply the highest risk ,classification,.

Classification of IVD medical devices
Classification of IVD medical devices

Software as in ,vitro diagnostic, medical devices (IVD s). The highest ,classification, determines the class of IVD Subregulation 3.3 (7) You must consider all of the ,classification, rules to determine the correct class of an IVD. If more than once ,classification, rule applies to your IVD, apply the highest risk ,classification,.

In-vitro Diagnostic Device Regulation (IVDR)
In-vitro Diagnostic Device Regulation (IVDR)

In-,vitro Diagnostic, Device Regulation IVDR Introduction IVDR. With the IVDR, the EU has issued a 157-page regulation which supersedes the IVD-Regulation (98/79/EC). The number of articles increased almost fivefold from 24 to 113.

Health and safety requirements for making and using clamp ...
Health and safety requirements for making and using clamp ...

During production, stainless steel uses scrap metal as its primary ,raw material,, with up to 70% of the product coming from recycled ,material,. Increased efficiency in process ,technology, has also decreased the amount of energy required to manufacture stainless steel.

Classification of IVD medical devices | Therapeutic Goods ...
Classification of IVD medical devices | Therapeutic Goods ...

7/12/2015, · This guidance on the ,classification of in-vitro diagnostic, medical devices (IVDs) is to assist manufacturers to classify their IVDs according to the Australian ,classification, rules …

Classification of Medical Devices and In Vitro Diagnostic ...
Classification of Medical Devices and In Vitro Diagnostic ...

A total of 350 categories of medical devices and 247 categories ,of in-vitro diagnostic, devices have been classified in accordance with the amended Annexure I as of the 6th of June 2018. Recently, on the 15th of May 2019, further ,classification, of 12 newly notified medical devices have been added to the existing list of classified devices.

MEDICAL DEVICE GUIDANCE
MEDICAL DEVICE GUIDANCE

classification of in vitro diagnostic, (IVD) medical devices using the appropriate risk ,classification, rules. 1.2. Background Regulatory controls should be proportional to the level of risk associated with an in ,vitro diagnostic, (IVD) medical device. The level of regulatory control

Basics of In-Vitro Diagnostic Medical Device Classification
Basics of In-Vitro Diagnostic Medical Device Classification

14/3/2015, · For the uninitiated, understanding the basics ,of In-Vitro Diagnostic, Medical Devices can be a confusing process. According to the 1998 medical device directive, IVDD 98/79/EC, an in-,vitro diagnostic, medical device (or IVD) is defined as “any medical device which is a reagent, reagent device, calibrator, control material, ,kit,, instrument, apparatus, equipment or system whether used alone or ...

The Best Clothing to Protect Against EMF/RF Radiation
The Best Clothing to Protect Against EMF/RF Radiation

2/5/2014, · It seems ,protective clothing, may be the best option. Here are a few ,clothing, products that provide shielding effects against EMF and RF radiation to significantly reduce exposure. Top 4 Garments and Products 1. Silver-lined ,clothing, by Silverell, Inc.

InVitro Diagnostics - CDSCO
InVitro Diagnostics - CDSCO

Classification, list ,of In Vitro Diagnostic, Medical Devices have been published on the website of the Central Drugs Standard Control Organisation approved by CLA. ... ,DIAGNOSTIC KIT, ( REGISTRATION CERTIFICATE) (IVD's) 2017-Feb-17: 135 KB: 5: USE OF RAPID TEST ,KITS, FOR TESTING OF HIV AND HCV IN BLOOD BANKS (IVD's) 2017-Feb-17: