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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.

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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.

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

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Consultation hotline:0086-15900663312

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

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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 ...

Aseptic Techniques in Microbiology - News-Medical.net
Aseptic Techniques in Microbiology - News-Medical.net

26/2/2019, · ,Aseptic, techniques refer to any ,method, used to sterilize and maintain the sterility of an object or location. ,Aseptic, procedures are used in microbiology.

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

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.

rapidmicrobiology Sampling and Testing Sterile Products
rapidmicrobiology Sampling and Testing Sterile Products

Sampling of ,sterile, products must be representative and must not allow any opportunities for accidental contamination and false positive results. Compendial sterility ,test methods, require 14-day incubation times, but rapid ,methods, have the potential to reduce that to five days or less.

Sterilizing Practices | Disinfection & Sterilization ...
Sterilizing Practices | Disinfection & Sterilization ...

The delivery of ,sterile, products for use in patient care depends not only on the effectiveness of the sterilization process but also on the unit design, decontamination, disassembling and packaging of the device, loading the sterilizer, monitoring, sterilant quality and quantity, and the appropriateness of the cycle for the load contents, and other aspects of device reprocessing.

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.

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 ...

Microbial Control and Monitoring in Aseptic Processing ...
Microbial Control and Monitoring in Aseptic Processing ...

If preferred, instead of the ,sterile, membrane filtration, a dilution series and plate count could be alternatively done. Personnel sampling. Periodic sampling of ,clothing, (gowns and gloves) is used to measure the effectiveness of ,aseptic, precautions.

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 …

rapidmicrobiology Sampling and Testing Sterile Products
rapidmicrobiology Sampling and Testing Sterile Products

Sampling of ,sterile, products must be representative and must not allow any opportunities for accidental contamination and false positive results. Compendial sterility ,test methods, require 14-day incubation times, but rapid ,methods, have the potential to reduce that to five days or less.

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 ...

Aseptic Techniques in Microbiology - News-Medical.net
Aseptic Techniques in Microbiology - News-Medical.net

26/2/2019, · ,Aseptic, techniques refer to any ,method, used to sterilize and maintain the sterility of an object or location. ,Aseptic, procedures are used in microbiology.

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 ...

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, ...

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 ...

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.

Medical Device & Pharmaceutical Sterility Testing ...
Medical Device & Pharmaceutical Sterility Testing ...

Method, suitability ,test, (Bacteriostasis and Fungistasis (B/F)) Minimization of inhibiting effects in ,test, (Neutralizing Antimicrobial activity)) Sterility testing on large or complex devices or products, for example, products exceeding a capacity of 20 liters per sample; Sterility testing is used for: ,Medical, …

ASTM D7103 - 19 Standard Guide for Assessment of Medical ...
ASTM D7103 - 19 Standard Guide for Assessment of Medical ...

D7907 ,Test Methods, for Determination of Bactericidal Efficacy on the Surface ,of Medical, Examination Gloves. F739 ,Test Method, for Permeation of Liquids and Gases Through Protective ,Clothing, Materials Under Conditions of Continuous Contact. F1342 ,Test Method, for Protective ,Clothing, Material Resistance to …