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Aimstep Ovulation

FDA UDI

Class I (US FDA UDI)

by Germaine Laboratories, Inc.

Identity

Trade Name
AIMSTEP OVULATION FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI
Device Name
A qualitative test to detect the LH surge in urine to aid in the prediction of ovulation. FDA UDI
Model / Reference
75030 FDA UDI
Description
A qualitative test to detect the LH surge in urine to aid in the prediction of ovulation. FDA UDI

Identifiers

Primary DI / UDI-DI
00695684750305 FDA UDI
FDA Product Code
CEP FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1485 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical

Aimstep Ovulation by Germaine Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 311aceea-c65f-4b31-90d6-000879dd3acb 33 fields · synced Jun 8, 2026