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T-Cup

FDA UDI

Class I (US FDA UDI)

by Wondfo Usa Co., Ltd.

Identity

Trade Name
T-Cup FDA UDI
Generic Name
General specimen container IVD, additive/medium FDA UDI
Device Name
T-Cup with Vaccu Lid,3 SVT strips (CR/pH/S.G.) and Temp Strip FDA UDI
Model / Reference
TDOA-SVTV FDA UDI
Description
T-Cup with Vaccu Lid,3 SVT strips (CR/pH/S.G.) and Temp Strip FDA UDI

Identifiers

Primary DI / UDI-DI
00816862024265 FDA UDI
FDA Product Code
NNI FDA UDI
GMDN Term
General specimen container IVD, additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen container IVD, additive/medium

T-Cup by Wondfo Usa Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 08db0b3a-c64d-4bf9-a17b-b37e9e58f0c4 35 fields · synced Jun 1, 2026