Laser pointer FDA certification How to do laser projector FDA registration

The head is one of the most important features of snake identification, so it is impossible to judge accurately. However, judging from the body color and pattern, it looks very similar to the sharp-scaled spearhead pither. Sharp-scaled protospearhead pitter, viper family, pit viper subfamily, protospearhead pit viper, highly venomous snake.

Commonly known as the king of rotten meat, as the name suggests, decay occurs near the wound. The head of the spearhead pit is typical of the long triangle shape, the neck is small, and the shape resembles a soldering iron, so it is called the soldering iron head. The body is slender, the tail is slender, it is entangled, and it is good at climbing trees.

It lives in hills and mountainous areas, inhabits bamboo forests, shrubs, streams, tea mountains, and cultivated land, and often goes to the grass around houses, garbage heaps, firewood, grass and stone crevices, and sometimes enters the house. It is distributed in Zhejiang, Anhui, Fujian, Taiwan, Jiangxi, Hunan, Guangdong, Guangxi, Hainan, Sichuan, Chongqing, Guizhou, Yunnan, Shaanxi and Gansu.

FDA registration must export laser products to the United States. There is no FDA, which means that you cannot pass through U.S. customs without approval from the U.S. FDA department, then your goods can only stay at the terminal or return.

What is the laser product registration process?

1.Samples 1-2pcs are provided

2.Provide product information.

3.Submit Information.

4.Audit data passed.

5.Closed. Information required for the laser head:

1.Application form.

2. Manual (English).

3. Circuit diagram (English).

4, Front and back of PCB, wiring diagram.

5. Component list, BOM list.

6. CD driver specifications (including laser wavelength range).

7. Laser path diagram, (line diagram) or JQA report from Japan.

8. Labels. <>

FDA Certification Process:

Fill in the application form, provide product information, and the registration is successful!

Turnaround time: 5-7 working days.

FDA certification process for laser products:

To apply for the FDA for laser products, you need to provide the following information:

1.Product Manual.

2.Laser test report.

3.Laser path diagram.

4.Production plant quality quality process.

5.Whole machine test, such as durability test, vibration test, high temperature and high humidity test, etc., 6Samples 1-2 pieces.

7.Laser pathway diagram.

8.Electronic file of label.

9.Quality assurance testing flow chart; Production, installation flow chart, the whole process from incoming materials to warehousing.

10.Whole machine test, such as durability test, vibration test, high temperature and high humidity test, etc.

There are many levels of this, Class 1, Class 2, Class 3, and you need to apply for FDA registration.

1.Application**,2English Instruction Manual, 3Circuit diagram, layout diagram, 5Component lists, movement specifications or JAQ reports, including laser wavelength ranges, 7Laser pathway diagram, 8Label electronic file, 9Quality assurance testing flow chart; Production, installation flow chart, the whole process from incoming materials to warehousing.

Laser projector FDA certification process:

Fill in the application form, provide product information, send samples over, test OK certificate Report period 5-7 working days.

FDA Certification Process: 1Submit application forms, samples and related information; 2.Testing, issuance of reports; 3.Submit to FDA for review; 4.The number is issued and the certificate is issued.