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kangzhou

FDA UDI

Class II (US FDA UDI)

by Weihai Kangzhou Biotechnology Engineering Co., Ltd

Identity

Trade Name
kangzhou FDA UDI
Generic Name
Cannabinoid/cannabinoid metabolite IVD, reagent FDA UDI
Model / Reference
cassette FDA UDI

Identifiers

Primary DI / UDI-DI
06923304623338 FDA UDI
FDA Product Code
PVJ FDA UDI
GMDN Term
Cannabinoid/cannabinoid metabolite IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3870 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cannabinoid/cannabinoid metabolite IVD, reagent

kangzhou by Weihai Kangzhou Biotechnology Engineering Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannabinoid/cannabinoid metabolite IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Weihai Kangzhou Biotechnology Engineering Co., Ltd

Sources (1)

  • FDA UDI 172bf7f9-85df-47d7-9dda-e88c0dba60c3 32 fields · synced Jun 8, 2026