Welcome to the company, we have many years of professional experience!
Chat
Online
Inquiry
Home > face mask non sterile

face mask non sterile

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

Certificate of Honor
CONTACT USCustomer satisfaction is our first goal!
Email us

Consultation hotline:0086-15900663312

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

face mask non sterile
Diagnostics : InVitro Technologies :: Cytocell
Diagnostics : InVitro Technologies :: Cytocell

The assay is supplied in a ,kit, format of 2, 5, 10 or 20 slides and includes hybridisation solution, counterstain, template slides, a hybridisation chamber and full ,instructions, for use. The ,kit, also contains a unique liquid crystal display slide surface thermometer for accurate measurement of the temperature of the denaturation surface.

In vitro diagnostic medical devices – Instructions for use ...
In vitro diagnostic medical devices – Instructions for use ...

Many microbiology and all microscopy products of Merck are “,in vitro diagnostic, medical devices” (IVD) according to the directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 and fulfill the requirements for CE self-certification.. ,Instructions, for Microbiology. We provide the general ,instruction, for use for dehydrated culture media and specific ,instructions, ...

OSOM ULTRA PLUS FLU A&B Control Kit INSTRUCTIONS FOR USE
OSOM ULTRA PLUS FLU A&B Control Kit INSTRUCTIONS FOR USE

Instructions, for use ,in vitro diagnostic, medical device Manufacturer Caution: Federal law restricts this device to sale by or on the order of a physician Uncontaminated recycled content-packaging, ,kit, box, ,Instructions, for Use is recyclable if it can be collected, separated, or otherwise recovered

In vitro diagnostic (IVD) devices: use safety and ...
In vitro diagnostic (IVD) devices: use safety and ...

Guidance for healthcare professionals covers the use, management and safety of ,in vitro diagnostic, (IVD) devices, including blood glucose meters.

Instruction for use IN VITRO DIAGNOSTIC
Instruction for use IN VITRO DIAGNOSTIC

For ,in vitro diagnostic, use It must be handled by specialized staff. Good laboratory and safety practices are advisable. Warning This ,kit, contains 125I emitting X and γ ionizing rays. This radioactive material may be received, acquired, possessed and used only by persons in clinical or hospital laboratories who are authorized by competent

IVD (In Vitro Diagnostic) Products: Overview Definitions ...
IVD (In Vitro Diagnostic) Products: Overview Definitions ...

A medical device is an ,in vitro diagnostic, medical device (IVD) if it is a reagent, calibrator, control material, ,kit,, specimen receptacle, software, instrument, apparatus, equipment or system, whether used alone or in combination with other ,diagnostic, goods for ,in vitro, use. It must be intended by the manufacturer to be used ,in vitro, for ..Read more

In vitro diagnostic medical devices – Instructions for use ...
In vitro diagnostic medical devices – Instructions for use ...

Many microbiology and all microscopy products of MilliporeSigma are “,in vitro diagnostic, medical devices” (IVD) according to the directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 and fulfill the requirements for CE self-certification.. ,Instructions, for Microbiology. We provide the general ,instruction, for use for dehydrated culture media and specific ...

D-10 Hemoglobin A1c Program Instruction Manual
D-10 Hemoglobin A1c Program Instruction Manual

23/9/2010, · 2 ,Instruction, Manual L20012105 INTENDED USE The Bio-Rad D-10™ Hemoglobin A1c Program is intended for the percent determination of hemoglobin A1c in human whole blood using ion-exchange high-performance liquid chromatography (HPLC). The Bio-Rad D-10 Hemoglobin A1c Program is intended for Professional Use Only. For ,In Vitro Diagnostic, Use.

ESBL ELITe MGB® Kit – ELITechGroup: In Vitro Diagnostic ...
ESBL ELITe MGB® Kit – ELITechGroup: In Vitro Diagnostic ...

ESBL ELITe MGB ® ,Kit, is a multiplex real-time PCR assay designed for the detection of CTX-M genes, the most prevalent group of ESBL genes in Enterobacteriaceae. The assay is CE-IVD validated on several sample matrices, in combination with ELITe InGenius ® , a fully automated sample-to-result solution.

Medical devices | European Medicines Agency
Medical devices | European Medicines Agency

A companion ,diagnostic, is an ,in-vitro diagnostic, test that supports the safe and effective use of a specific medicinal product, by identifying patients that are suitable or unsuitable for treatment.. The ,In-Vitro Diagnostic, Devices Regulation introduces a new classification system for companion ,diagnostics, and the obligation to undergo a conformity assessment by a notified body.