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FIRSTVIEW Fentanyl Urine Test Cassette

FDA UDI

Class II (US FDA UDI)

by Safecare Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
FIRSTVIEW Fentanyl Urine Test Cassette FDA UDI
Generic Name
Fentanyl IVD, kit, rapid ICT, clinical FDA UDI
Model / Reference
5 tests FDA UDI

Identifiers

Catalog Number
FYL-1012 FDA UDI
Primary DI / UDI-DI
06974246461496 FDA UDI
510(k) Number
K240654 FDA UDI
FDA Product Code
NGL FDA UDI
GMDN Term
Fentanyl IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3650 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fentanyl IVD, kit, rapid ICT, clinical

FIRSTVIEW Fentanyl Urine Test Cassette by Safecare Biotech (Hangzhou) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fentanyl IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI be897601-acc1-40b6-9a46-a2616cca53fb 34 fields · synced May 30, 2026