Identity
- Trade Name
- Rapid TOX FDA UDI
- Generic Name
- Amphetamine/methamphetamine group IVD, calibrator FDA UDI
- Device Name
- RapidTOX Methamph single 50/cs FDA UDI
- Model / Reference
- 10-METT-000 FDA UDI
- Description
- RapidTOX Methamph single 50/cs FDA UDI
Identifiers
- Catalog Number
- 10-METT-000 FDA UDI
- Primary DI / UDI-DI
- 10694644100355 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
- Amphetamine/methamphetamine group 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: Amphetamine/methamphetamine group IVD, calibrator
Rapid TOX by American Bio Medica Corp. — 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
- American Bio Medica Corp.
Sources (1)
- FDA UDI 589bd1b8-e5a0-4d5d-a764-a37390600afd 36 fields · synced Jun 8, 2026