Identity
- Trade Name
- QuikStrip Multidrug Screening Dip Card Test FDA UDI
- Generic Name
- Drug/toxicology screen adulteration IVD, kit, rapid spectrophotometry, clinical FDA UDI
- Device Name
- QuikStrip Multidrug 5 Test, AMP 500, COC 300, MET 500, OP I 2000, THC 50 FDA UDI
- Model / Reference
- 30500 FDA UDI
- Description
- QuikStrip Multidrug 5 Test, AMP 500, COC 300, MET 500, OP I 2000, THC 50 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00748349000373 FDA UDI
- FDA Product Code
- LDJ FDA UDIDJG FDA UDIDJC FDA UDIDIO FDA UDIDKZ FDA UDI
- GMDN Term
- Drug/toxicology screen adulteration IVD, kit, rapid spectrophotometry, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3870 FDA UDI862.3650 FDA UDI862.3610 FDA UDI862.3250 FDA UDI862.3100 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
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: Drug/toxicology screen adulteration IVD, kit, rapid spectrophotometry, clinical
QuikStrip Multidrug Screening Dip Card Test by Syntron Bioresearch, 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
- Syntron Bioresearch, Inc.
Sources (1)
- FDA UDI b4545dd6-0da8-4670-9d69-00b19e472277 33 fields · synced May 30, 2026