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n95 4-layer filter mask

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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CONTACT USCustomer satisfaction is our first goal!
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Consultation hotline:0086-15900663312

Address:No. 3888, Hutai Road, Baoshan District, Shanghai, China

n95 4-layer filter mask
Trademark basics | USPTO
Trademark basics | USPTO

25/9/2020, · What ,you, should know before filing The trademark application process is a legal proceeding governed by U.S. law. If ,you, are a foreign-domiciled applicant, ,you, must have a U.S.-licensed attorney represent ,you, at the USPTO.; If ,you, are an applicant domiciled in the ,United States,, ,you, are not required to have a U.S.-licensed attorney represent ,you,, but we strongly encourage ,you, to hire one who ...

If You’re Going to Wear a Mask to Protect Yourself From ...
If You’re Going to Wear a Mask to Protect Yourself From ...

When it comes ,to the United States,’s handling of the ... and N95s can only be produced in ,FDA,-approved factories—the CFDA encouraged ... “,You need, to treat your mask like workout ,clothes,.

Importing Goods & Wholesale Products to USA | SaleHoo
Importing Goods & Wholesale Products to USA | SaleHoo

The first thing ,you need, to ,do, is contact a supplier and let them know your business plan. Don't forget to ask for the requirements needed for selling their items. If ,you, decide to purchase items in bulk (or by container load), a customs broker may be needed to handle tariffs, and other import/export regulations.

DHL | US FDA Regulations | English
DHL | US FDA Regulations | English

Registration, of Facilities: The ,FDA, will require that domestic and foreign facilities that manufacture, process, pack, or hold food for human or animal consumption in the ,United States register, with the ,FDA,.

Personal Protective Equipment - Overview | Occupational ...
Personal Protective Equipment - Overview | Occupational ...

Personal ,protective, equipment, commonly referred to as "PPE", is equipment worn to minimize exposure to hazards that cause serious workplace injuries and illnesses. These injuries and illnesses may result from contact with chemical, radiological, physical, electrical, mechanical, or other workplace hazards.

Doing Business As (DBA): What Is It and Is It Needed ...
Doing Business As (DBA): What Is It and Is It Needed ...

Some people change their names for personal or professional reasons. The commercial version of this is called Doing Business As (DBA). A company uses a DBA when the name it operates under is different from its legal, registered name.

We get Personal Protective Equipment to those who need it ...
We get Personal Protective Equipment to those who need it ...

Through our coalition of data scientists, makers, partners and donors, Get Us PPE has amassed the largest non-governmental database of PPE shortages in the ,United States,. This data is critical for helping our nonprofit organization get personal ,protective, equipment where it is needed most. Help us get PPE into critical areas.

FDA Registration - Hand sanitizer
FDA Registration - Hand sanitizer

Even though the manufacturer follows the guidance, they ,need, to comply with ,FDA Registration,, NDC labeler code and hand sanitizer listing requirements. If ,you, are looking for assistance in preparing and submitting SPL files for antiseptic drug products, LMG can help ,you, in SPL preparation and submission to ,FDA,.

Restrictions on Genetically Modified Organisms: United States
Restrictions on Genetically Modified Organisms: United States

Drugs developed through genetic engineering must ,go, through the same NDA process as other types of drugs. 4. Biological Products. The ,FDA, also regulates medical products classified as “biological products,” which includes vaccines, serums, blood products, and the like, under relevant provisions of the Public Health Service Act (PHSA).

Statutes | CPSC.gov
Statutes | CPSC.gov

The CNPPA requires any nicotine provided in a liquid nicotine container sold, offered for sale, manufactured for sale, distributed in commerce, or imported into the ,United States, to be in “special packaging” as defined by the PPPA and in accordance with the Commission’s regulations at 16 C.F.R. §§ 1700.15 and 1700.20.

Frequently Asked Questions about Copyright | U.S ...
Frequently Asked Questions about Copyright | U.S ...

What ,do, I ,do, if I am unable to submit an application or a required physical copy due to the pandemic and I ,need, to ,register, to preserve statutory damages? How ,do, I know whether I should use a Deposit Ticket Declaration Form or a 710 Declaration?

Clothing and Textiles | Federal Trade Commission
Clothing and Textiles | Federal Trade Commission

Garment labels give consumers important purchasing information. If ,you, manufacture, import or sell fur garments — whether coats, capes, stoles or parkas — ,you, must comply with the labeling requirements under the Fur Products Labeling Act (FPLA). This guidance explains the FPLA’s current requirements.

If You’re Going to Wear a Mask to Protect Yourself From ...
If You’re Going to Wear a Mask to Protect Yourself From ...

When it comes ,to the United States,’s handling of the ... and N95s can only be produced in ,FDA,-approved factories—the CFDA encouraged ... “,You need, to treat your mask like workout ,clothes,.

Restrictions on Genetically Modified Organisms: United States
Restrictions on Genetically Modified Organisms: United States

Drugs developed through genetic engineering must ,go, through the same NDA process as other types of drugs. 4. Biological Products. The ,FDA, also regulates medical products classified as “biological products,” which includes vaccines, serums, blood products, and the like, under relevant provisions of the Public Health Service Act (PHSA).

Frequently Asked Questions - ClinicalTrials.gov
Frequently Asked Questions - ClinicalTrials.gov

The Final Rule preamble ,states,: "[A] clinical study of a device product that is being conducted entirely outside of the ,United States, (i.e., does not have any sites in the ,United States, or in any U.S. territory) and is not conducted under an IDE may not be a clinical study of a device product subject to section 510(k), 515, or 520(m) of the FD&C Act and, therefore, is not an applicable device ...