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GL GoodLife Glucose Control Solutions

FDA UDI

Class I (US FDA UDI)

by Hmd Biomedical, LLC

Identity

Trade Name
GL GoodLife Glucose Control Solutions FDA UDI
Generic Name
Glucose IVD, control FDA UDI
Device Name
GL GoodLife Glucose Control Solution FDA UDI
Model / Reference
3C-01-160032 FDA UDI
Description
GL GoodLife Glucose Control Solution FDA UDI

Identifiers

Catalog Number
3C-01-160032 FDA UDI
Primary DI / UDI-DI
00389154000549 FDA UDI
510(k) Number
K113307 FDA UDI
FDA Product Code
JJX FDA UDI
LFR FDA UDI
NBW FDA UDI
GMDN Term
Glucose IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
862.1345 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

GL GoodLife Glucose Control Solutions by Hmd Biomedical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 24d16c22-4bba-4589-bbac-be7367ecc221 38 fields · synced May 30, 2026