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Difference between industrial and medical goggles

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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Difference between industrial and medical goggles
New EU regulations on medical devices: What changes from ...
New EU regulations on medical devices: What changes from ...

26/5/2020, · The present regulations (set in the late 1990s) ,do, not guarantee the ,registration, of a drug-,device, combination product. Discrepancies in the categorization of MDs across Europe is also frequent. Due to the lack of specific guidelines, the location of data and amount of published information related to the ,device, element varies across companies.

State Regulation of Medical Device Distribution
State Regulation of Medical Device Distribution

License/Registration Requirements. Th e most consistent state requirement for medical device distributors is the requirement to be licensed or registered with the state. However, the . process. for obtaining such licensure/registration varies signifi cantly among the states, making advance planning a necessity for companies launching their fi rst

Frequently Asked Questions on Medical Device Regulation ...
Frequently Asked Questions on Medical Device Regulation ...

5/5/2017, · ,Devices, holding a ,certificate, from a European Notified Body under either the ,Medical Device, Directive (93/42/EEC) or the Active Implantable ,Medical Devices, Directive (90/385/EEC) have an additional grace period and may continue to be placed on the market until 26 May 2024 if the manufacturer fulfil the specific prerequisite requirements drawn in the MDR.

Class 1 Medical Devices - Johner Institute
Class 1 Medical Devices - Johner Institute

This step is also obvious: Manufacturers of class 1 ,medical devices, must also affix the CE marking. In the case of class 1* ,medical device,, the CE marking must be accompanied by the identification number of the relevant notified body. Step 7: ,Registration, of ,devices, and manufacturers in EUDAMED. However, the seventh step is new in its current form.

Medical Devices Interim Regulation - SFDA
Medical Devices Interim Regulation - SFDA

Medical Devices, National Registry (MDNR): is the database of registered establishments and the ,medical devices, they manufacture or import or distribute. National Center for ,Medical Device, Reporting (NCMDR): is an organization managing a database of information on safety and performance related aspects of ,medical devices

Certificate of FDA Registration - fdahelp.us
Certificate of FDA Registration - fdahelp.us

A 510(K) Premarket Notification is only for ,medical device,, if you are a ,medical device, manufacturer and your ,device, classification is 510k, you can submit a 510k notification to FDA, it may take 3-6 months to complete a 510k review. If you are looking for a ,certificate, as a proof of FDA ,registration, for your customers, please Contact us

Brazil Medical Device Approval & ANVISA Registration
Brazil Medical Device Approval & ANVISA Registration

Brazil is the largest ,medical device, market in Latin America, with an established but complex regulatory system. ,Medical devices, in Brazil are regulated by the Agência Nacional de Vigilância Sanitária (ANVISA). Brazil's base regulations and ,medical device, classification schemes are similar to those found in the European MDD 93/42/EEC.

What will be the requirements for the importation of ...
What will be the requirements for the importation of ...

For ,medical device, that is for ,registration,, a special certification will be issued stating that the product to be imported will be issued as a sample only for ,registration,. F or exempted ,medical devices,, a ,certificate, of listing will be issued prior to the importation of the ,device,.

HSA | Regulatory overview of cosmetic products
HSA | Regulatory overview of cosmetic products

Cosmetic product manufacturers in Singapore ,do, not require a manufacturer’s licence. However, the manufacturer may apply for a Good Manufacturing Practice (GMP) ,certificate, to facilitate the export of the cosmetic products. Refer to our guide on GMP certification for more details on how to apply.

Class 1 Medical Devices - Johner Institute
Class 1 Medical Devices - Johner Institute

This step is also obvious: Manufacturers of class 1 ,medical devices, must also affix the CE marking. In the case of class 1* ,medical device,, the CE marking must be accompanied by the identification number of the relevant notified body. Step 7: ,Registration, of ,devices, and manufacturers in EUDAMED. However, the seventh step is new in its current form.