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safe mask pro review

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.

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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safe mask pro review
Information for Filing PPE and Medical Devices during COVID-19
Information for Filing PPE and Medical Devices during COVID-19

Under this Intended Use Code, the Affirmations of Compliance for ,medical, devices (such as the ,Registration,, Listing, and Premarket numbers) are optional in ACE. Below is a list of products and ...

Guidance on the Import of Hand Sanitisers Masks ...
Guidance on the Import of Hand Sanitisers Masks ...

Any protective gear for ,medical, professionals e.g. ,isolation, gowns and gloves (1) Import for Commercial and/or other purposes (not for personal use): If you are importing these ,medical, devices for commercial or other purposes (e.g. workplace use, donation), please submit a …

Important regulatory considerations for the supply of ...
Important regulatory considerations for the supply of ...

For information about the ,licensing, or authorization of ,medical, devices in Canada, contact the ,Medical, Devices Directorate at hc.meddevices-instrumentsmed.sc@canada.ca. Health Canada is also fast-tracking the MDEL application process for companies that want to manufacture, import or distribute Class I ,medical, gowns.

Personal Protective Equipment against COVID-19: Medical ...
Personal Protective Equipment against COVID-19: Medical ...

Companies with a ,medical, device establishment licence (MDEL) can import and distribute ,medical, gowns. The COVID-19 pandemic has created an unprecedented demand for ,medical, gowns. To meet the demand, Health Canada is: easing approvals of ,medical, devices through an Interim Order,

Malaysia medical device registrations | TÜV SÜD PSB
Malaysia medical device registrations | TÜV SÜD PSB

Understanding the regulatory framework for ,medical, devices in Malaysia - MDA and MDAA. Passed in 2012, the ,Medical, Device Act (MDA) and the ,Medical, Device Authority Act (MDAA) represent the first efforts by Malaysia to implement mandatory safety requirements for ,medical, devices marketed or sold in that country. Regulations under the MDA replaced the country’s voluntary product ,registration, ...

Disposable Isolation Gowns
Disposable Isolation Gowns

28/4/2020, · certification of ,registration, annex to cert. no.: listing no code 2006us116558 device name non*urgical ,isolation, gown (nonsurgical ,isolation, gown) mask, scavenging mask) accessory. surgical apparel (accessory,surgicai.apparel, face mask) cap. surgical (cap,surgical) cover, shoe. operating-room (shoe cover) bedding disposable. ,medical, gown ...

HSA | Registration overview of medical devices
HSA | Registration overview of medical devices

Registration, requirements ,Registration, requirements. Refer to the table below for an overview of the evaluation routes for Class B, C and D ,medical, devices. A ,medical, device without prior approval from any of our overseas reference regulatory agencies must undergo a full evaluation.

Andaman Medical | Medical Device Regulatory Requirements ...
Andaman Medical | Medical Device Regulatory Requirements ...

All information and documents submitted for the ,registration, of Class B, C and D ,medical, devices have to comply with the ASEAN Common Submission Dossier Template (CSDT) format. All ,registration, submissions must be provided in English and the applicant must ensure that the non-English information (e.g information on label) is complete, accurate, unbiased and consistent with English information.

Registration of Medical Device and Medical equipment
Registration of Medical Device and Medical equipment

Registration, process of ,Medical, Devices or ,Medical, Equipment Duration*: When registering products of class 1 and 2A — 330 calendar days / 11 months; class 2b and 3 — 400 calendar days / 13 months. * excluding clock-stops (time to eliminate Authority questions) Including clock-stops at …

Department of Health - Registration of Healthcare ...
Department of Health - Registration of Healthcare ...

Main ,Service, Areas ,Registration, of Healthcare Professionals. Under existing legislation, the following healthcare professionals are required to be registered with their respective boards or councils before they are allowed to practise in Hong Kong.