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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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.
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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 …
For information about the ,licensing, or authorization of ,medical, devices in Canada, contact the ,Medical, Devices Directorate at firstname.lastname@example.org. Health Canada is also fast-tracking the MDEL application process for companies that want to manufacture, import or distribute Class I ,medical, gowns.
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,
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, ...
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 ...
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.
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, 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 …
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.