What is FDA product code PUZ?

The benzodiazepine test is an in vitro diagnostic test for the qualitative analysis of benzodiazepines for employment and insurance testing. FDA has exempted these devices from the premarket notification requirement by publishing in the Federal Register of July 11, 2017 (82 FR 31976) available at https://www.federalregister.gov/documents/2017/07/11/2017-14453/medical-devices-exemptions-from-premarket-notification-class-ii-devices subject to the limitations under 21 CFR XXX.9, where XXX refers to Parts 862-892, and any limitations on the exemption described in (82 FR 31976). Any device that exceeds the limitations found in 21 CFR sections 862.9 to 892.9 or identified in the Federal Register (82 FR 31976) available at https://www.federalregister.gov/documents/2017/07/11/2017-14453/medical-devices-exemptions-from-premarket-notification-class-ii-devices is required to submit a premarket

Clinical Chemistry › Toxicology Test SystemsTest, Benzodiazepine, Employment And Insurance Testing, Exempt

Rapid Response

Name: Rapid Response
Brand: Rapid Response

Rapid Response 5 Panel Saliva Test Cup E/I Screening (D5.1.1-2FC1E)-THC40 COC20 AMP50 MET50 OPI40. For employment and insurance testing.

Registry build 21.09.26

11manufacturers in China registered for this device type

1catalogue number

Who Else Makes It

Concentrated in Zhejiang (6), Guangdong (3), Beijing (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code PUZ
Manufacturer	City	Province	Registered as	Device types
Zhejiang Orient Gene Biotech	Huzhou	Zhejiang	Contract manufacturer	86
Hangzhou AllTest Biotech Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	48
Assure Tech. (Hangzhou) Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	48
Guangzhou Wondfo Biotech Co., Ltd.	Guangzhou	Guangdong	Contract manufacturer	44
Hangzhou Biotest Biotech Co., Ltd.	Hangzhou	Zhejiang	Contract manufacturer	41
W.h.p.m. Bioresearch & Technology Co., Ltd.	Beijing	Beijing	Manufacturer	37
Guangzhou Decheng Biotechnology Co., Ltd.	Guangzhou	Guangdong	Complaint-file establishment	35
Eterbio, Inc.	Zhuhai	Guangdong	Manufacturer	29
Weihai Kangzhou Biotechnology Engineering Co., Ltd.	Weihai	Shandong	Manufacturer	24
Hangzhou Lysun Biotechnology Co., Ltd.	Hangzhou	Zhejiang	Manufacturer	22
Hangzhou Tongzhou Biotechnology Co., Ltd.	Hangzhou	Zhejiang	Manufacturer	14

Record

Regulatory record for Rapid Response
Listed by	Btnx Inc., Canada
FDA product code	PUZ
Device type	Test, Benzodiazepine, Employment And Insurance Testing, Exempt
Device class	Class 2
Regulation	21 CFR 862.3170
Establishment	Repacker / relabeller, Private-label distributor, Complaint-file establishment, Exporter
Record published	2022-12-07
Record revised	2023-04-20 (version 2)

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

Catalogue Numbers

Catalogue numbers for Rapid Response
Catalogue number	Size	Per pack	Status
D5.1.1-2FC1E		25	In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
iScreen™	Instant Technologies, Inc.	1

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.