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.
Does Shantou have the factory that makes protective clothing
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.
Professional team work and production line which can make nice quality in short time.
The professional team provides 24 * 7 after-sales service for you, which can help you solve any problems
Address：No. 3888, Hutai Road, Baoshan District, Shanghai, China
Medical gloves, are ,disposable gloves, used during ,medical, examinations and procedures to help prevent cross-contamination between caregivers and patients. ,Medical gloves, are made of different polymers including latex, nitrile rubber, polyvinyl chloride and neoprene; they come unpowdered, or powdered with corn starch to lubricate the ,gloves,, making them easier to put on the hands.
April 6, 2020 – Canada Border Services Agency (CBSA) recently issued Custom Notice CN20-12 providing guidelines to the commercial importing industry on tariff classifications (HS code) and other useful information on ,medical, supplies and certain manufacturing inputs related to COVID-19. A list of ,medical, supplies for COVID-19 based on HS ,classification, provided by the World... Read more »
A ,medical device classification, system is therefore needed, in order to channel ,medical devices, into the proper conformity assessment route. In order to ensure that conformity assessment under the ,Medical Device, Directive functions effectively from January 1995, manufacturers should be able to know as early as possible in which class their product is.
If you have elected to demonstrate compliance with the Regulation, the ,Medical Device, Regulation (MDR) No. 2017/745 (for ,medical devices, or active implantable ,medical devices,) or the In Vitro Diagnostic ,Device, Regulation (IVDR) No. 2017/746 would be considered.
HPRA Guide to ,Classification, of a ,Medical Device, 4.2 ,Classification, rules . There are eighteen rules outlined in Annex IX of the Directive and related Regulation that lay down the basic principles of ,classification,. In MEDDEV 2.4/1 Rev. 8, these rules are further …
The EU MDR 2017/745 has 4 main categories for ,Medical Devices classification,:. Class I; Class IIa; Class IIb; Class III; This goes from the products with low risk (Class I) to the products with high risk (Class III). You can find this on the MDR 2017/745 (to be precise – Chapter V Section 1 Article 51). But if you want to be more specific, we can say that there are 3 sub-classes under class I.
20/12/2018, · The FDA classifies ,medical devices, in over 1700 generic ,device, categories within 16 ,medical, specialties. Each ,classification, outlines a unique compliance based on risk estimates. (1) A ,medical device, is recognized in the official National Formulary, or the US Pharmacopeia, or Formulary, or the US Pharmacopeia, or any supplement to them.
Surgical rubber ,gloves, 4015.11 Other rubber ,gloves,. 4015.19 Knitted or crocheted ,gloves, which have been impregnated or covered with plastics or rubber 6116.10 Textile ,gloves, that are not knitted or crocheted 6216.00 Other ,Disposable, hair nets 6505.00 Protective garments for surgical/,medical, …