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GlucoLeader Enhance Blood Glucose Test Strip

FDA UDI

Class II (US FDA UDI)

by Hmd Biomedical, LLC

Identity

Trade Name
GlucoLeader Enhance Blood Glucose Test Strip FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
GlucoLeader Enhance GL Blood Glucose Test Strip FDA UDI
Model / Reference
GL vial FDA UDI
Description
GlucoLeader Enhance GL Blood Glucose Test Strip FDA UDI

Identifiers

Primary DI / UDI-DI
04711200722864 FDA UDI
510(k) Number
K032985 FDA UDI
FDA Product Code
CGA FDA UDI
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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Glucose monitoring system IVD, home-use

GlucoLeader Enhance Blood Glucose Test Strip by Hmd Biomedical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hmd Biomedical, LLC

Sources (1)

  • FDA UDI 58c2cd2c-d3e6-4493-900b-c1eb1c160b17 34 fields · synced May 30, 2026