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GL GoodLife Blood Glucose Meter AC-11

FDA UDI

Class II (US FDA UDI)

by Hmd Biomedical, LLC

Identity

Trade Name
GL GoodLife Blood Glucose Meter AC-11 FDA UDI
Generic Name
Glucose monitoring system IVD, home-use FDA UDI
Device Name
GL GoodLife Blood Glucose Meter (single patient home use) FDA UDI
Model / Reference
3K-01-16003S FDA UDI
Description
GL GoodLife Blood Glucose Meter (single patient home use) FDA UDI

Identifiers

Catalog Number
3K-01-16003S FDA UDI
Primary DI / UDI-DI
00389154000679 FDA UDI
510(k) Number
K113307 FDA UDI
FDA Product Code
LFR FDA UDI
JJX 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
862.1660 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

GL GoodLife Blood Glucose Meter AC-11 by Hmd Biomedical, LLC — Class II — 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 66437950-86e9-4b7f-8c38-1f19dbfe77f8 37 fields · synced May 30, 2026