Identity
- Trade Name
- Rapid TOX FDA UDI
- Generic Name
- Propoxyphene IVD, calibrator FDA UDI
- Device Name
- Rapid Tox Propoxyphene 50/case FDA UDI
- Model / Reference
- 10-PPXT-000 FDA UDI
- Description
- Rapid Tox Propoxyphene 50/case FDA UDI
Identifiers
- Catalog Number
- 10-PPXT-000 FDA UDI
- Primary DI / UDI-DI
- 10694644100348 FDA UDI
- FDA Product Code
- LCM FDA UDILFG FDA UDILDJ FDA UDIJXN FDA UDIDJG FDA UDIDJR FDA UDIDJC FDA UDIDIO FDA UDIJXM FDA UDIDIS FDA UDIDKG FDA UDI
- GMDN Term
- Propoxyphene IVD, calibrator FDA UDI
Classification
- Device Class
- U FDA UDI
- Regulation Number
- 862.3910 FDA UDI862.3870 FDA UDI862.3700 FDA UDI862.3650 FDA UDI862.3620 FDA UDI862.3610 FDA UDI862.3250 FDA UDI862.3170 FDA UDI862.3150 FDA UDI862.2270 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
Category: Propoxyphene IVD, calibrator
Rapid TOX by American Bio Medica Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Propoxyphene IVD, calibrator.
- Pointe Propoxyphene (PPX) Calibrator (300 ng/mL) Cutoff — POINTE SCIENTIFIC, INC. · Class II
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- Propoxyphene DAU Calibrator, Low Calibrator — Lin-Zhi International, Inc. · Class II
- Propoxyphene DAU Calibrator, Intermediate Calibrator — Lin-Zhi International, Inc. · Class II
- Pointe Propoxyphene (PPX) Calibrator (600 ng/mL) Intermediate — POINTE SCIENTIFIC, INC. · Class II
- Pointe Propoxyphene (PPX) Calibrator (1000 ng/mL) High — POINTE SCIENTIFIC, INC. · Class II
- Pointe Propoxyphene (PPX) Calibrator (150 ng/mL) Low — POINTE SCIENTIFIC, INC. · Class II
- Propoxyphene DAU Calibrator, Cutoff Calibrator — Lin-Zhi International, Inc. · Class II
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
- American Bio Medica Corp.
Sources (1)
- FDA UDI 3cc69683-751c-4bc0-b269-de00bdf1fd0a 36 fields · synced Jun 1, 2026