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Teco Diagnostics

FDA UDI

Class II (US FDA UDI)

by Teco Diagnostics

Identity

Trade Name
TECO DIAGNOSTICS FDA UDI
Generic Name
Urine blood IVD, kit, rapid colorimetric, clinical FDA UDI
Device Name
URS-1B-100 BOTTLE ONLY FDA UDI
Model / Reference
URS-1B-100 BOTTLE FDA UDI
Description
URS-1B-100 BOTTLE ONLY FDA UDI

Identifiers

Catalog Number
URS-1B-100B FDA UDI
Primary DI / UDI-DI
10673486000139 FDA UDI
510(k) Number
K023297 FDA UDI
FDA Product Code
JIO FDA UDI
GMDN Term
Urine blood IVD, kit, rapid colorimetric, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6550 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

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: Urine blood IVD, kit, rapid colorimetric, clinical

Teco Diagnostics by Teco Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urine blood IVD, kit, rapid colorimetric, clinical.

Cleared under the same submission

K023297 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teco Diagnostics

Sources (1)

  • FDA UDI 2c70a051-1838-4b39-9db0-df512141a27c 36 fields · synced May 30, 2026