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Equate

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
Equate FDA UDI
Generic Name
Natural conception assistance kit FDA UDI
Device Name
A convenience kit consisting of 10 Equate Early Ovulation Test devices and 1 Equate One Step Pregnancy Test. FDA UDI
Model / Reference
Early Ovulation Kit FDA UDI
Description
A convenience kit consisting of 10 Equate Early Ovulation Test devices and 1 Equate One Step Pregnancy Test. FDA UDI

Identifiers

Primary DI / UDI-DI
00681131240789 FDA UDI
510(k) Number
K042280 FDA UDI
K981271 FDA UDI
FDA Product Code
LCX FDA UDI
CEP FDA UDI
GMDN Term
Natural conception assistance kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 FDA UDI
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

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: Total human chorionic gonadotropin IVD, kit, rapid ICT, clinicalNatural conception assistance kit

Equate by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Natural conception assistance kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walmart Stores

Sources (1)

  • FDA UDI 45cee2d5-f5b2-4917-95f5-a4e2b6ac3469 36 fields · synced May 30, 2026