Identity
- Trade Name
- Meijer FDA UDI
- Generic Name
- Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- A convenience kit consisting of 1 Digital Pregnancy Test and 1 Early Result Pregnancy Test FDA UDI
- Model / Reference
- Digital & Early Result Pregnancy Tests FDA UDI
- Description
- A convenience kit consisting of 1 Digital Pregnancy Test and 1 Early Result Pregnancy Test FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00719283842732 FDA UDI
- FDA Product Code
- LCX FDA UDI
- GMDN Term
- Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1155 FDA UDI
- Commercial Distribution
- Not 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
Meijer by Meijer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K042280 also covers:
- Care One — Ahold U.S.A., Inc.
- Discount Drug Mart One Step Pregnancy Test — DISCOUNT DRUG MART, INC.
- Rexall — DOLGENCORP, LLC
- Rexall — DOLGENCORP, LLC
- H.E.B — H. E. BUTT GROCERY COMPANY
- Kroger — KROGER CO., THE
- Kroger — KROGER CO., THE
- Kroger — KROGER CO., THE
- Kroger — KROGER CO., THE
- Meijer — MEIJER, INC.
- Meijer — MEIJER, INC.
- Sunmark Pregnancy Test One Step — Mckesson Corp.
K060128 also covers:
- CareOne — Ahold U.S.A., Inc.
- Amazon — Amazon.com Services, LLC
- Albertsons — BETTER LIVING BRANDS LLC
- H.E.B — H. E. BUTT GROCERY COMPANY
- H.E.B — H. E. BUTT GROCERY COMPANY
- H.E.B — H. E. BUTT GROCERY COMPANY
- Kroger — KROGER CO., THE
- Kroger — KROGER CO., THE
- Meijer — MEIJER, INC.
- Clearblue — SPD SWISS PRECISION DIAGNOSTICS GMBH
- Equaline — SPD SWISS PRECISION DIAGNOSTICS GMBH
- Equaline Digital Pregnancy Test — SPD SWISS PRECISION DIAGNOSTICS GMBH
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Meijer, Inc.
Sources (1)
- FDA UDI d1cf2cc2-b7b2-4b22-ac6b-7f6d95d85f38 37 fields · synced Jun 1, 2026