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0574-27880028

Ningbo KPL Technology Co., Ltd.

Mr.Chen    :18668299419

Mr.Huang  :13056889909

Mr.Wang   :15067891153

Miss Geng :15088816300
Miss Hu     : 15906559403

Advice or complaint:0574-27880028

U.S . FDA authentication

release time :2021-12-24 14:32:11    

1 Introduction

        FDA ( Food and ) Brief Introduction

        Food and FDA for short )

        FDA is the United States Government Department of Health and Human Services ( DHHS ) and the Ministry of Public Health ( PHS ) in the establishment of one of the implementing agencies .

        As a scientific management mechanism , FD ^ of duties is to ensure that the dollar national production or imports of food , medical care and it is assumed that each of the radiation safety of the product . It is the earliest to protect consumption as the main functions of federal agencies ( Hua ) , cosmetics , drugs , biological agents ,

        medical equipment and product safety . It is the earliest in order to protect consumers as the main functions of federal agencies . The agency and every American ' s life , and . at the international level , the FDA was recognized as the world ' s largest food and drug agency .

 

2 . The approval mark

3 Technical Information

        laser products with the FDA to do frequency voltage Guan is not large

        providing a desired wavelength of the laser head

         

4 product range

        food products

        medical products

        cosmetics

        radiation electronic products ( KPL )

        Nutrient health - care product

        Chinese herbal medicine and medicine

        health care equipment

        canned food

         

5 Factory inspection

        does not require factory inspection

6 Instruction for authentication

        I can do the FDA Division of laser products , laser - like cosmetic , neutraceutical , etc with a touch of the human body of the product is likely to meet the costs of the products according to the FDA application , if the customer does not understand , should remind the customer to select the correct category of the Food and Drug Administration ( FDA ) .

         

        Most imports out of the locals know . . the US FDA for the management of food , medicines , Cen products , medical equipment , jade - pipe organ , but sometimes many unwary radia1ion emitting radiation emitting products ( product ) is also one of the department ' s products .

        FDA regulations f of the source of radiation emitting products is The Federal Food , Drug , and Cosmetics Act , Part 5 , 531 - 542 ( FEDERAL FOOD , AND , ACT , referred to simply as FD . Zhuo called for the release of radiation of an electronic product , including a screen with a television antenna , microwave , X - ray diagnostic apparatus and X - rays or laser - related products ( such as CD - ROM and the laser pointer ( 1aser poin1cr ) etc . ) . Most radiation emitting products which are not identified as She treatment equipment , but the manufacturing or distributors claim that the products have a medical function , and the products shall comply with the FDA on medical device ( s ) specifications . Congressional legislation led to the release of radiation of an electronic main reason is to prevent consumers from the use of such products to health .

        1 . A self - proclaimed conform to Table

        2 . Product Registration

        3 . Test Standard

        4 . Product reporting ( ProductRepor1s )

        5 . annual reports ) (

        welcome to the annual report from September 1 to the FDA , as not regularly updated , the products will be held up in customs clearance . If the operator inadvertently fails to timely mail the report other than that of the detention , the customs may accept the vendor and the additional associated information after customs clearance .

        6 . Test record

        7 . Relevant records

        8 . The provisions of the warning signs

         

7 certification data and process

        Preparation and delivery of : the need for customer product specification ( English ) , the circuit diagram , PCB , such as the sample does not need to provide the laser head is allowed to remove bad picture

         

Certification Process

        1 . Application Form submitted , with samples and related data

        2 . Test report

        3 . to submit to the FDA review

        4 . review by number sending , license - issuing

        5 . In the ACC and the rest of the payment claim them . No files

         

8 - certification

        4 - 5 weeks .