Identity
- Trade Name
- MP DOA-6 TEST CUP 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: AMP / BZD / COC / OPI / OXY / THC FDA UDI
- Model / Reference
- 07RD7112-08 FDA UDI
- Description
- Immunoassay for the detection of the following drug substance(s) in human urine: AMP / BZD / COC / OPI / OXY / THC FDA UDI
Identifiers
- Catalog Number
- 07RD7112-08 FDA UDI
- Primary DI / UDI-DI
- 00817830020487 FDA UDI
- FDA Product Code
- DIO FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3250 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
- Height — 74 Millimeter FDA UDI
Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Mp Doa-6 Test Cup by Rapid Diagnostics Inc — 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
- Rapid Diagnostics Inc
Sources (1)
- FDA UDI ee9a038f-fea4-4392-aa77-edc250a63c5c 37 fields · synced May 31, 2026