What is FDA product code PUY?

The barbiturate test is an in vitro diagnostic test for the qualitative analysis of barbiturates 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 notif

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

UScreen®

Name: UScreen®
Brand: UScreen®

UScreen Drug Test Cup, Employment And Insurance Testing, Exempt: AMP, MET, BAR, BZO BUP, COC, OPI, OXY, THC, K2 (CR, pH, OX).

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 PUY
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 UScreen®
Listed by	Instant Technologies, Inc.
FDA product code	PUY
Device type	Test, Barbiturate, Employment And Insurance Testing, Exempt
Device class	Class 2
Regulation	21 CFR 862.3150
Premarket notification	Exempt
Record published	2018-02-09
Record revised	2022-06-10 (version 5)

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 4 to 30 °C

Catalogue Numbers

Catalogue numbers for UScreen®
Catalogue number	Size	Status
USSCupA-10K2		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
T-Cube®	Instant Technologies, Inc.	2
Amazewell	Guangzhou Decheng Biotechnology Co., Ltd.	2

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.