Identity
- Trade Name
- Rite Aid FDA UDI
- Generic Name
- Cocaine/cocaine metabolite IVD, reagent FDA UDI
- Device Name
- Home Drug Test 4 Panel COC/OPI/mAMP/THC FDA UDI
- Model / Reference
- 8024510 FDA UDI
- Description
- Home Drug Test 4 Panel COC/OPI/mAMP/THC FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00011822001663 FDA UDI
- FDA Product Code
- NFY FDA UDINGL FDA UDINGG FDA UDINFW FDA UDI
- GMDN Term
- Cocaine/cocaine metabolite IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3250 FDA UDI862.3650 FDA UDI862.3610 FDA UDI862.3870 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
No
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: Cannabinoid/cannabinoid metabolite IVD, reagentCocaine/cocaine metabolite IVD, reagentOpiate/opiate metabolite IVD, reagentMethamphetamine-specific IVD, reagent
Rite Aid by Rite Aid Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Rite Aid Corporation
Sources (1)
- FDA UDI 77554b39-74a3-4b93-9cfb-5951799b1d19 33 fields · synced Jun 8, 2026