Identity
- Trade Name
- DOA 1 PANEL TEST FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- Immunoassay for the detection of the following drug substance(s) in human urine: PCP FDA UDI
- Model / Reference
- 07RD7060-09 FDA UDI
- Description
- Immunoassay for the detection of the following drug substance(s) in human urine: PCP FDA UDI
Identifiers
- Catalog Number
- 07RD7060-09 FDA UDI
- Primary DI / UDI-DI
- 00817830020746 FDA UDI
- FDA Product Code
- LCM FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- U 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
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 75 Millimeter FDA UDI
Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Doa 1 Panel Test by Rapid Diagnostics Inc — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Rapid Diagnostics Inc
Sources (1)
- FDA UDI a30014cd-9228-42c8-b3e9-a8bb219fc342 37 fields · synced Jun 8, 2026