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Meijer Ovulation Test - Easy One Step

FDA UDI

Class I (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
MEIJER OVULATION TEST - EASY ONE STEP FDA UDI
Generic Name
Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
One-step ovulation predictor test used for the detection of Luteininzing Hormone (LH) in urine to predict your time of ovulation. FDA UDI
Model / Reference
16919 FDA UDI
Description
One-step ovulation predictor test used for the detection of Luteininzing Hormone (LH) in urine to predict your time of ovulation. FDA UDI

Identifiers

Primary DI / UDI-DI
00760236169192 FDA UDI
FDA Product Code
CEP FDA UDI
GMDN Term
Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay 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, chemiluminescent immunoassay

Meijer Ovulation Test - Easy One Step by Meijer, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luteinizing hormone (LH) IVD, kit, chemiluminescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI 0cb7c7da-c207-4a14-85be-5532849e7a1e 35 fields · synced May 29, 2026