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INSTANT-VIEW LH Ovulation Predicting Dip-Strip Test

FDA UDI

Class I (US FDA UDI)

by Alfa Scientific Designs, Inc.

Identity

Trade Name
INSTANT-VIEW LH Ovulation Predicting Dip-Strip Test FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical FDA UDI
Device Name
INSTANT-VIEW LH Ovulation Predicting Dip-Strip Test FDA UDI
Model / Reference
02-2547 FDA UDI
Description
INSTANT-VIEW LH Ovulation Predicting Dip-Strip Test FDA UDI

Identifiers

Primary DI / UDI-DI
10796918000122 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

INSTANT-VIEW LH Ovulation Predicting Dip-Strip Test by Alfa Scientific Designs, 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 f0f9ab36-8972-47f4-90bb-c2392d4037bc 33 fields · synced Jun 9, 2026