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Cartoon of protective clothing with simple strokes

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

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Cartoon of protective clothing with simple strokes
HSA | Medical devices
HSA | Medical devices

Before you continue: You are encouraged to check if your product is considered a ,medical device, in Singapore.; You will need to determine your ,medical device,’s risk ,classification,.; If your ,medical device's, risk ,classification, is ,Class, B, C or D, you should check if your ,device, has been approved by our overseas reference regulatory agencies.; If you know your product's evaluation route and ...

Ophthalmic Medical Devices | BSI
Ophthalmic Medical Devices | BSI

The ,Medical Device, Directive includes a ,classification, system based on the degree of perceived risk associated with the ,device,. There are four classes: ,Class, I covers ,devices, considered to be low risk (may include ,devices, such as corrective glasses and frames, eye occasion plasters, permanent magnets for removal of ocular debris)

Catalogue of medical device classification code and name
Catalogue of medical device classification code and name

Catalogue, of ,medical device classification, code and name No. Code Category Name (CN) Category Name (EN) Related Products(Partial) Latest update d 1 6801 基础外科手 术器械 Basic surgical instruments Vessel dilator, Scalp clip System, dermal curette, dissecting forceps, Dissector 2002 2 6802 显微外科手 术器械 Microsurgical

New NMPA-Catalogue for Medical Devices
New NMPA-Catalogue for Medical Devices

New NMPA-,Catalogue, for ,Medical Devices, The NMPA (China Food and Drug Administration) published a new ,classification catalog, on 31.08.2017 (No. 2017-104). The new ,catalog,, with more than 2,000 entries of product ,classifications,, is much more extensive than the previous ,catalog,, which featured only around 200 product examples.

Guidelines for Classification of Medical Devices - CE ...
Guidelines for Classification of Medical Devices - CE ...

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.

Ophthalmic Medical Devices | BSI
Ophthalmic Medical Devices | BSI

The ,Medical Device, Directive includes a ,classification, system based on the degree of perceived risk associated with the ,device,. There are four classes: ,Class, I covers ,devices, considered to be low risk (may include ,devices, such as corrective glasses and frames, eye occasion plasters, permanent magnets for removal of ocular debris)

New Medical Device Classification Catalog CFDA China
New Medical Device Classification Catalog CFDA China

On August 1, 2018, China Food and Drug Administration (CFDA) - the Chinese health authority, has taken a major step towards ,classification, of ,medical devices, to be marketed or currently being marketed in China. The CFDA has officially published and mandated the new ,Medical Device Classification Catalog,. To be on par with continuous changes in regulations for ,medical devices, and considering the ...

New Medical Device Classification Catalog CFDA China
New Medical Device Classification Catalog CFDA China

On August 1, 2018, China Food and Drug Administration (CFDA) - the Chinese health authority, has taken a major step towards ,classification, of ,medical devices, to be marketed or currently being marketed in China. The CFDA has officially published and mandated the new ,Medical Device Classification Catalog,. To be on par with continuous changes in regulations for ,medical devices, and considering the ...

HSA | Medical devices
HSA | Medical devices

Before you continue: You are encouraged to check if your product is considered a ,medical device, in Singapore.; You will need to determine your ,medical device,’s risk ,classification,.; If your ,medical device's, risk ,classification, is ,Class, B, C or D, you should check if your ,device, has been approved by our overseas reference regulatory agencies.; If you know your product's evaluation route and ...

What classification is my medical device? | Therapeutic ...
What classification is my medical device? | Therapeutic ...

Medical devices, are classified according to the level of harm they may pose to users or patients. The following tool will assist in determining the ,classification, of a ,medical device, that is not an In Vitro Diagnostic ,device,.There are separate ,classification, rules for IVD ,devices,.

Catalogue of medical device classification code and name
Catalogue of medical device classification code and name

Catalogue, of ,medical device classification, code and name No. Code Category Name (CN) Category Name (EN) Related Products(Partial) Latest update d 1 6801 基础外科手 术器械 Basic surgical instruments Vessel dilator, Scalp clip System, dermal curette, dissecting forceps, Dissector 2002 2 6802 显微外科手 术器械 Microsurgical

Classify Your Medical Device | FDA
Classify Your Medical Device | FDA

For ,Class, III ,devices,, a premarket approval application (PMA) will be required unless your ,device, is a preamendments ,device, (on the market prior to the passage of the ,medical device, amendments in ...

Did You Know That Sunglasses Are Regulated by The FDA As ...
Did You Know That Sunglasses Are Regulated by The FDA As ...

30/5/2019, · The Product Code is assigned to the ,medical device, according to the ,classification, of the ,device,. The Product Code assigned to a ,device, is based upon the ,medical device, product ,classification, designated under 21 CFR Parts 862-892. the product code assists CBP officers, FDA officials, importers, and etc. in accurately identifying the ,class, in which the ,medical device, falls under and in tracking ...

Catalogue of medical device classification code and name
Catalogue of medical device classification code and name

Catalogue, of ,medical device classification, code and name No. Code Category Name (CN) Category Name (EN) Related Products(Partial) Latest update d 1 6801 基础外科手 术器械 Basic surgical instruments Vessel dilator, Scalp clip System, dermal curette, dissecting forceps, Dissector 2002 2 6802 显微外科手 术器械 Microsurgical

New Medical Device Classification Catalog Issued by the ...
New Medical Device Classification Catalog Issued by the ...

At present, China has approximately 77,000 ,medical device, registration certificates and 3.7 million ,medical, equipment records, making the process of obtaining, tracking and managing ,classification, documentation a rather large feat. On September 4, 2017, in an effort to simplify the ,classification, process, the China Food and Drug Administration introduced a new version of the “,Medical Device, ...

Classify Your Medical Device | FDA
Classify Your Medical Device | FDA

For ,Class, III ,devices,, a premarket approval application (PMA) will be required unless your ,device, is a preamendments ,device, (on the market prior to the passage of the ,medical device, amendments in ...

Guidance on class 1 medical devices - GOV.UK
Guidance on class 1 medical devices - GOV.UK

Guidance on ,class, 1 ,medical devices,. This guidance applies to manufacturers of ,class, I ,medical devices,, including accessories but excluding ,devices, intended for clinical investigation and custom ...

Catalogue Downloads - Dentec Safety
Catalogue Downloads - Dentec Safety

Dentec Safety First Aid ,Catalogue, English (PDF) 2019 Dentec Eye Brochure English (PDF) 2019 Dentec Eye Brochure French (PDF) ... Dentec Safety ICETRED™ Traction ,Devices, Literature French (PDF) Dentec Safety Specialists, Inc. 195 B Harry Walker Parkway North, Newmarket, ON L3Y 7B3