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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
01
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.

02
Highly specialized team and products

Professional team work and production line which can make nice quality in short time.

03
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.

04
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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WHO | Personal protective equipment for COVID-19
WHO | Personal protective equipment for COVID-19

Technical, specifications for personal protective equipment and related infection prevention and control supplies can be find below. COVID-19 ,Technical, Specifications for personal protective equipment pdf, 356kb; Rational use of personal protective equipment for coronavirus disease (COVID-19)

WHO | Personal protective equipment for COVID-19
WHO | Personal protective equipment for COVID-19

Technical, specifications for personal protective equipment and related infection prevention and control supplies can be find below. COVID-19 ,Technical, Specifications for personal protective equipment pdf, 356kb; Rational use of personal protective equipment for coronavirus disease (COVID-19)

Medical Device Directive (MDD)
Medical Device Directive (MDD)

Essential ,requirements, • Article 4 . Free movement, devices intended for special purposes • Article 5 . Reference to standards • Article 6 . Committee on standards and ,technical, regulations • Article 7 . Committee on ,Medical, Devices • Article 8 . Safeguard clause • Article 9 . Classification • Article 10 . Information on incidents ...

Medical Device Directive 93/42/EEC| TÜV SÜD
Medical Device Directive 93/42/EEC| TÜV SÜD

Manufacturers of currently approved ,medical, devices will have a transition time of three years until May 26th 2021 (date of application) to meet the ,requirements, of the MDR. The new MDR provides an additional time after the date of application allowing to place new products under the MDD for max. 4 more years on the market.

Provisions for Medical Device Registration
Provisions for Medical Device Registration

Chapter III Product ,Technical Requirements, and Registration Testing. Article 15 The applicant or filing entity shall prepare the product ,technical requirements for medical, device to be registered or filed. The product ,technical requirements, for class I ,medical, devices shall be submitted to the food and drug regulatory department at the time of ...

Requirements for Updating a Medical Device Technical File
Requirements for Updating a Medical Device Technical File

22/5/2020, · Hi, I understand that part of the CE marking ,requirements, for a ,medical, device is to hold a ,Technical, File for the device in the EU. Most of this file will come from documents in our Device Master Record (DMR). I was wondering if anyone knows the ,requirements, for updating the ,Technical,...

E-health Support in People with Parkinson's Disease with ...
E-health Support in People with Parkinson's Disease with ...

To provide guidelines for developers in creating new PD applications for smart ,glasses,, a self-reported questionnaire was designed to survey the ,requirements,, constraints, and attitudes of people with PD with respect to this new technology. The survey was advertised online over an 11 month period on the website of the Parkinson Vereninging.

Standards of Medical Examination for Executive Posts ...
Standards of Medical Examination for Executive Posts ...

Back Standards of ,Medical, Examination for Executive Posts (,Technical, & Non-,Technical,), in DMRC:-The candidate recommended ,for medical, examination will have to pass ,medical, fitness test(s) conducted by the DMRC Administration to ensure that the candidates are medically fit in all respects to carry out the duties connected with the post.

Lead Glasses | Radiation Glasses | Leaded Eyewear
Lead Glasses | Radiation Glasses | Leaded Eyewear

Beyond frame color options, many of our radiation safety ,glasses, offer optional lens enhancements, such as fog-free and anti-reflective coatings or prescription Rx lenses. Whether for your hospital, dental practice, or X-ray lab, protect your eyes with a comfortable pair of our lead ,glasses,.

Technical Documentation Requirements under the MDR – a ...
Technical Documentation Requirements under the MDR – a ...

Moving on this point, a ,Technical, File under the MDR must include a rationale why a product is a ,medical, device and also justify in detail which risk class is applicable. Furthermore, a manufacturer has to give reference to previous and similar device generations and provide extended design process details including information about suppliers and subcontractors.

What's the Difference Between Industrial and Medical Grade ...
What's the Difference Between Industrial and Medical Grade ...

Medical, Grade and Surgical Grade gloves, which are fundamentally synonymous terms, have to pass a series of ,technical, tests to see if they meet the safety ,requirements, put forth by the FDA. Gloves are tested for puncture and abrasion resistance, they are run through tension and elongation tests, and are also tested for chemical substance resistance.

China Regulatory Consulting for Medical Device
China Regulatory Consulting for Medical Device

The Guideline on Preparation of ,Medical, Device ,Technical Requirements,; Special Review and Approval Procedure for Innovative ,Medical, Devices; Introduction to ,Technical, Guiding Principle on ,Medical, Devices Clinical Evaluation; ... 2020-03-02 [Case Study] ,Medical, Isolation ,Goggles, (Eye Masks ...

Eye and Face Protectors : OSH Answers
Eye and Face Protectors : OSH Answers

Lenses: CSA-certified eye and face protectors must meet the criteria for impact resistance as outlined in the standard.Only devices made of approved materials are permitted. Markings: The manufacturer or supplier certification mark must be present on all approved safety lenses, frames (front and temple), removable side shields, and other parts of the ,glasses,, ,goggles,, or helmets.

Personal Protective Equipment (PPE)
Personal Protective Equipment (PPE)

EYE PROTECTION: ,Goggles, are required when working with batteries, gasoline, or solvents. Safety ,glasses, or ,goggles, must be worn when grinding, or performing hot work tasks. Welding helmet or shaded ,goggles, must be worn when welding or using torch. Whenever the potential exists for flying chips, burrs, or debris to enter the eye

Medical Device Overview | FDA
Medical Device Overview | FDA

Overview. This page provides an overview of ,medical, devices and the ,requirements, that the FDA verifies/enforces at the time they are imported or offered for import into the United States.

Medical Device Regulation (MDR)| TÜV SÜD
Medical Device Regulation (MDR)| TÜV SÜD

5/5/2017, · Manufacturers of currently approved ,medical, devices will have a transition time of three years until May 26th 2020 (postponed to May 26 th 2021) to meet the ,requirements, of the regulation. For some manufacturers the new regulation provides an additional time after the date of application allowing them to place new products for max. 4 more years on the market.

WHO | WHO Technical Specification for Medical Devices
WHO | WHO Technical Specification for Medical Devices

WHO ,Technical, Specifications for 13 ,Medical, Devices on UN Life-Saving Commodities. The WHO ,technical, specification for 61 ,medical, devices was developed in accordance with essential ,medical, devices needed by the health care facilities. It was complied by WHO in collaboration with a working group of experts.

Regulations & Guidelines
Regulations & Guidelines

Regulating ,medical, devices, in vitro- diagnostic devices, prescription eye ,glasses,, contact lenses and their solutions, are among the responsibilities of SFDA in accordance with its law issued by the royal decree No.(M/6) issued on 13/2/2007.