← Back to catalogue

u-Cup

FDA UDI

Class II (US FDA UDI)

by Ucp Biosciences, Inc.

Identity

Trade Name
u-Cup FDA UDI
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Device Name
10 Panel Drug Test Cup BAR/BUP/BZO/COC/MET/MTD/OPI/OXY/TCA/THC with Adulteration strip(S.G.,CRE, pH) FDA UDI
Model / Reference
U-DUD-7104 FDA UDI
Description
10 Panel Drug Test Cup BAR/BUP/BZO/COC/MET/MTD/OPI/OXY/TCA/THC with Adulteration strip(S.G.,CRE, pH) FDA UDI

Identifiers

Catalog Number
U-DUD-7104 FDA UDI
Primary DI / UDI-DI
10817038021412 FDA UDI
FDA Product Code
DJR FDA UDI
DJC FDA UDI
DKZ FDA UDI
DJG FDA UDI
DIO FDA UDI
LDJ FDA UDI
JXM FDA UDI
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3620 FDA UDI
862.3610 FDA UDI
862.3100 FDA UDI
862.3650 FDA UDI
862.3250 FDA UDI
862.3870 FDA UDI
862.3170 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

Yes

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: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

u-Cup by Ucp Biosciences, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple drugs of abuse IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Ucp Biosciences, Inc.

Sources (1)

  • FDA UDI 0493da90-ae46-4776-a9f4-1ff1cedb154b 35 fields · synced May 30, 2026