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Home > Protective clothing without shoe cover

Protective clothing without shoe cover

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

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

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 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

24 / 7 guaranteed service

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

Certificate of honor


CONTACT USCustomer satisfaction is our first goal!

Consultation hotline:0086-15900663312

Address:No. 3888, Hutai Road, Baoshan District, Shanghai, China

Protective clothing without shoe cover

Cleanroom Wipe Testing Standards for ASTM IEST & ISO ...

Cleanroom Wipe Testing Standards for ASTM IEST & ISO ...

13/2/2020, · ISO 9073-10:2005-03 Textiles – ,Test Methods, for Nonwovens – Part 10: Lint and other particle generation in the dry state.. ISO 14698-1 and ISO 14698-3 – Standards which address suitable procedures for cleaning and disinfection. ISO 10993 covers the biological evaluation ,of medical, devices for toxicity.Inherently, understanding the potential toxicity of a product or device must also ...

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The New Standard for Barrier Surgical Gowns and Drapes ...

The New Standard for Barrier Surgical Gowns and Drapes ...

With the pressing need for a ,test method,, an industry-driven committee of theAmerican Society for Testing Materials (ASTM) released a modification of one ofits existing mechanical devices that had originally been developed fordetermining the effectiveness of protective ,clothing, worn by chemical workers.The group incorporated the methodology in two tests; one for liquid penetrationand one for ...

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Bioburden Testing Method Facts | Wickham Labs | UK Testing ...

Bioburden Testing Method Facts | Wickham Labs | UK Testing ...

This testing is used to measure the total aerobic microbial count (TAMC) on ,medical, devices prior to any final stages of sterilisation or implantation use. Bioburden testing for ,medical, devices made or used worldwide is governed by ISO 11737 or in the USA by Title 21 …

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Updated guidance on packaging for terminally-sterilized ...

Updated guidance on packaging for terminally-sterilized ...

Therefore, they can be applicable to ,medical, device manufacturer, a health care facility, or an organization that reprocesses ,medical, devices. BS EN ISO 11607-1 and -2 were revised in 2019. Both standards give requirements covering ,medical, device protection, the ability to sterilize, maintenance of ,sterile, package integrity and ,aseptic, ...

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Packaging for terminally sterilized medical devices

Packaging for terminally sterilized medical devices

4.4 ,Test methods, ... 7 Usability evaluation for ,aseptic, presentation ... combined to create a ,sterile medical, device that performs efficiently, safely and effectively in the hands of the user. This document specifies requirements for the design of ,sterile, barrier systems and packaging systems

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Microbiological Evaluation of Sterile Medical Devices

Microbiological Evaluation of Sterile Medical Devices

Test, of Sterility not to be confused with a Sterility ,Test, • Specifically used in sterilisation process validation ,of medical, devices • Uses only one media –non selective, nutrient rich eg TSB. Incubated for 14 days at 28-30OC. • Products cannot be pooled, 10 individual products must be tested. At least 9 out of 10 products should show ...

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EN 13795-1 - European Standards

EN 13795-1 - European Standards

EN 13795-1 EN 13795-1 Surgical ,clothing, and drapes - Requirements and ,test methods, - Part 1: Surgical drapes and gowns - Original English text of CSN EN Standard. The price of the Standard included all amendments and correcturs.

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VALIDATING MEDICAL DEVICE PACKAGING - UL

VALIDATING MEDICAL DEVICE PACKAGING - UL

test, reports that validate packaging stability using accelerated aging studies, pending receipt of data from real-time aging assessments. Accelerated aging studies are normally conducted in accordance with the standardized ,test methods, described in ASTM F 1980, Standard Guide for Accelerated Aging of ,Sterile Medical, Device Packages.

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Be compliant by selecting the right sterile cleanroom ...

Be compliant by selecting the right sterile cleanroom ...

right ,sterile, cleanroom ,clothing, solution ... prietary ,Clean,-Donhnology ensures gowning is simple to learn and ... F is the general ,test method, used to conduct chemical permeation testing, ASTM D˙ includes some additional requirements speci c to chemotherapy drugs.

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Quality Control Analytical Methods: Microbial Limit Tests ...

Quality Control Analytical Methods: Microbial Limit Tests ...

ble Number (MPN). The MPN ,method, is reserved for TAMC in low bioburden samples, and is not suitable for the estima-tion of fungal recovery. USP chapTer <61> ,meThod, suiTabiliTy ,TesT, (,meThod, ValidaTioN) The suitability ,test, is conducted to dem-onstrate the applicability of the ,method, for detection of microbial contamination in the ,test, product.

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