Identity
- Trade Name
- AccuSign® OPI card FDA UDI
- Generic Name
- Opiate/opiate metabolite IVD, kit, rapid ICT, clinical FDA UDI
- Device Name
- AccuSign® OPI card; 35 Test kit; CE FDA UDI
- Model / Reference
- DOA-203-35-02 FDA UDI
- Description
- AccuSign® OPI card; 35 Test kit; CE FDA UDI
Identifiers
- Catalog Number
- DOA-203-35-02 FDA UDI
- Primary DI / UDI-DI
- 10743816000082 FDA UDI
- FDA Product Code
- DJG FDA UDI
- GMDN Term
- Opiate/opiate metabolite IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3650 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
Yes
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: Opiate/opiate metabolite IVD, kit, rapid ICT, clinical
AccuSign® OPI card by Princeton Biomeditech Corp. — 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
- Princeton Biomeditech Corp.
Sources (1)
- FDA UDI 84b03187-308c-4cd2-8d42-000c45e01137 36 fields · synced May 30, 2026