← Back to catalogue

T-Cup®

FDA UDI

Class U (US FDA UDI)

by Instant Technologies, Inc.

Identity

Trade Name
T-Cup® FDA UDI
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Device Name
T-Cup® Multi-Drug Urine Test Cup with Adulterants (CR, NI, pH, OX, SG) 7 panel AMP1000, COC300, MET500, OPI300, OXY100, PCP25, THC50 FDA UDI
Model / Reference
TDOA-7A FDA UDI
Description
T-Cup® Multi-Drug Urine Test Cup with Adulterants (CR, NI, pH, OX, SG) 7 panel AMP1000, COC300, MET500, OPI300, OXY100, PCP25, THC50 FDA UDI

Identifiers

Primary DI / UDI-DI
00817405021086 FDA UDI
510(k) Number
K182701 FDA UDI
FDA Product Code
NGM FDA UDI
NFW FDA UDI
NGL FDA UDI
NGG FDA UDI
NFY FDA UDI
NFT FDA UDI
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
U FDA UDI
Regulation Number
862.3870 FDA UDI
862.3650 FDA UDI
862.3610 FDA UDI
862.3250 FDA UDI
862.3100 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

Yes

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

T-Cup® by Instant Technologies, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

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

Sources (1)

  • FDA UDI 717778d6-f167-45c7-95d0-13b01b3cbb75 36 fields · synced May 30, 2026