← Back to catalogue

DIABIMETRICS Blood Glucose Monitoring System

FDA UDI

Class II (US FDA UDI)

by Health For Mankind Company

Identity

Trade Name
DIABIMETRICS Blood Glucose Monitoring System FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
Meter*1 Lancing Device*1 Sterile Lancets*10 FDA UDI
Model / Reference
TD-4143 FDA UDI
Description
Meter*1 Lancing Device*1 Sterile Lancets*10 FDA UDI

Identifiers

Primary DI / UDI-DI
00860009958012 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose monitoring system IVD, home-use 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose monitoring system IVD, home-use

DIABIMETRICS Blood Glucose Monitoring System by Health For Mankind Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose monitoring system IVD, home-use.

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 650b3d88-7b34-444a-af9f-8d1ce5ef758d 33 fields · synced May 29, 2026