Henry Schein

Rapid test for the quantitative detection of Influenza A&B antigens in nasal swab specimens

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Zhejiang. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code GNX
Manufacturer City Province Registered as Device types
Hangzhou Rollmed Co., Ltd. Hangzhou Zhejiang Contract manufacturer 127

Record

Regulatory record for Henry Schein
Listed by Henry Schein, Inc., United States
FDA product code GNX
Device type Antigens, Cf (Including Cf Control), Influenza Virus A, B, C
Device class Class 1
Regulation 21 CFR 866.3330
Record published 2016-09-24
Record revised 2022-06-10 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 30 °C; Special storage condition: No
Packaging Pack of 27

Catalogue Numbers

Catalogue numbers for Henry Schein
Catalogue number Size Status
1126219 In distribution

Same Product Code

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Product Sold by Catalogue numbers
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Showing 12 of 22. All products under Antigens, Cf (Including Cf Control), Influenza Virus A, B, C

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer