Identity
- Trade Name
- Rite Aid FDA UDI
- Generic Name
- Cannabinoid/cannabinoid metabolite IVD, reagent FDA UDI
- Device Name
- Home Drug Test 7 Panel THC/COC/OPI/PCP/mAMP/AMP/MDMA FDA UDI
- Model / Reference
- 8024511 FDA UDI
- Description
- Home Drug Test 7 Panel THC/COC/OPI/PCP/mAMP/AMP/MDMA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00011822001694 FDA UDI
- FDA Product Code
- NFW FDA UDINFY FDA UDINGL FDA UDINGM FDA UDINGG FDA UDINFT FDA UDI
- GMDN Term
- Cannabinoid/cannabinoid metabolite IVD, reagent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3870 FDA UDI862.3250 FDA UDI862.3650 FDA UDI862.3610 FDA UDI862.3100 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: Amphetamine/methamphetamine group IVD, kit, rapid ICT, clinicalCannabinoid/cannabinoid metabolite IVD, reagentCocaine/cocaine metabolite IVD, reagentOpiate/opiate metabolite 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 8cefbe7c-303d-492f-84f8-c79f53a68a2d 33 fields · synced May 30, 2026