Identity
- Trade Name
- Verify FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- mLife Verify Oral Fluid Drug Test AMP-COC-MET-OPI-PCP-THC-MDMA-OXY-ALC FDA UDI
- Model / Reference
- M320901 FDA UDI
- Description
- mLife Verify Oral Fluid Drug Test AMP-COC-MET-OPI-PCP-THC-MDMA-OXY-ALC FDA UDI
Identifiers
- Primary DI / UDI-DI
- G474M3209010 FDA UDI
- FDA Product Code
- PVJ FDA UDIPUX FDA UDIPVA FDA UDIPVD FDA UDIPUZ FDA UDIPVH FDA UDIPVC FDA UDIPUY FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3870 FDA UDI862.3100 FDA UDI862.3250 FDA UDI862.3610 FDA UDI862.3170 FDA UDI862.3650 FDA UDI862.3580 FDA UDI862.3150 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
No
FDA UDI
Convenience Kit
No
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
Verify by Mlife Diagnostics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mlife Diagnostics Llc
Sources (1)
- FDA UDI a8d574a8-6c08-4065-a678-9625657268e6 36 fields · synced May 30, 2026