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Aimstrip Plus Blood Glucose Meter, Box Kit

FDA UDI

Class II (US FDA UDI)

by Germaine Laboratories, Inc.

Identity

Trade Name
AIMSTRIP PLUS BLOOD GLUCOSE METER, BOX KIT FDA UDI
Generic Name
Home-use blood glucose spot-check system FDA UDI
Device Name
A blood glucose meter for use with AimStrip® Plus Blood Glucose Test Strips for testing blood glucose levels. FDA UDI
Model / Reference
37321 FDA UDI
Description
A blood glucose meter for use with AimStrip® Plus Blood Glucose Test Strips for testing blood glucose levels. FDA UDI

Identifiers

Primary DI / UDI-DI
00695684373214 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Home-use blood glucose spot-check system 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

No

FDA UDI

Category: Home-use blood glucose spot-check system

Aimstrip Plus Blood Glucose Meter, Box Kit by Germaine Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use blood glucose spot-check system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Germaine Laboratories, Inc.

Sources (1)

  • FDA UDI b5efc267-34b7-48d7-8d95-f6c4aa041e90 33 fields · synced May 30, 2026