← Back to catalogue

Tenovi

FDA UDI

Class II (US FDA UDI)

by Tenovi Co

Identity

Trade Name
Tenovi FDA UDI
Generic Name
Glucose IVD, reagent FDA UDI
Device Name
Glucometer Test Strips (50 Pack) FDA UDI
Model / Reference
TE-STR-A1 FDA UDI
Description
Glucometer Test Strips (50 Pack) FDA UDI

Identifiers

Primary DI / UDI-DI
00860008115911 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose IVD, reagent

Tenovi by Tenovi Co — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose IVD, reagent.

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
Tenovi Co

Sources (1)

  • FDA UDI 7e9aedf2-ef2d-4cea-bb0b-a5a93554be98 33 fields · synced May 30, 2026