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.
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
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The professional team provides 24 * 7 after-sales service for you, which can help you solve any problems
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 ...Get Price Send E-mail
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 ...Get Price Send E-mail
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 …Get Price Send E-mail
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, ...Get Price Send E-mail
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 systemsGet Price Send E-mail
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 ...Get Price Send E-mail
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.Get Price Send E-mail
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.Get Price Send E-mail
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.Get Price Send E-mail
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.Get Price Send E-mail