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Easy@Home Ovulation Test Strip (bulk)

FDA UDI

Class I (US FDA UDI)

by Easy Healthcare Corporation

Identity

Trade Name
Easy@Home Ovulation Test Strip (bulk) FDA UDI
Generic Name
Natural conception assistance kit FDA UDI
Device Name
LH test strips in bulk package FDA UDI
Model / Reference
EZW2-S FDA UDI
Description
LH test strips in bulk package FDA UDI

Identifiers

Primary DI / UDI-DI
00855944007093 FDA UDI
FDA Product Code
CEP FDA UDI
GMDN Term
Natural conception assistance kit 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

Yes

FDA UDI

Convenience Kit

Yes

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: Natural conception assistance kit

Easy@Home Ovulation Test Strip (bulk) by Easy Healthcare Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Natural conception assistance kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f824a7fc-5df1-4994-95a1-5897564dd0a7 33 fields · synced Jun 8, 2026