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Aimstrip Hemoglobin Optical Verifiers

FDA UDI

Class I (US FDA UDI)

by Germaine Laboratories, Inc.

Identity

Trade Name
AIMSTRIP HEMOGLOBIN OPTICAL VERIFIERS FDA UDI
Generic Name
Haemoglobin detection IVD, calibrator FDA UDI
Device Name
AimStrip® Hb Optical Verifiers are made out of plastic and work with the AimStrip® HB Hemoglobin (Hb) Meter. FDA UDI
Model / Reference
78102 FDA UDI
Description
AimStrip® Hb Optical Verifiers are made out of plastic and work with the AimStrip® HB Hemoglobin (Hb) Meter. FDA UDI

Identifiers

Primary DI / UDI-DI
00695684781026 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Haemoglobin detection IVD, calibrator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haemoglobin detection IVD, calibrator

Aimstrip Hemoglobin Optical Verifiers by Germaine Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e8ba2365-e4eb-4e81-a6b9-2bbe7b45d2d5 33 fields · synced May 30, 2026