Identity
- Trade Name
- Verify FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- mLife Verify 9 Panel Oral Fluid Drug Test AMP BAR BZO COC MDMA MET MTD OPI OXY FDA UDI
- Model / Reference
- MV002.09.0004EI FDA UDI
- Description
- mLife Verify 9 Panel Oral Fluid Drug Test AMP BAR BZO COC MDMA MET MTD OPI OXY FDA UDI
Identifiers
- Primary DI / UDI-DI
- G474MV002090004EI0 FDA UDI
- FDA Product Code
- PVB FDA UDIPUZ FDA UDIPVJ FDA UDIPUX FDA UDIPVA FDA UDIPVD FDA UDIPVH FDA UDIPUY FDA UDIPVC FDA UDIPVE FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3270 FDA UDI862.3170 FDA UDI862.3870 FDA UDI862.3100 FDA UDI862.3250 FDA UDI862.3610 FDA UDI862.3650 FDA UDI862.3150 FDA UDI862.3580 FDA UDI862.3620 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
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
Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Verify by Mlife Diagnostics Llc — 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
- Mlife Diagnostics Llc
Sources (1)
- FDA UDI ddef1ee2-b674-4fc5-9420-70f3adfc65b2 35 fields · synced May 30, 2026