Identity
- Trade Name
- Discover FDA UDI
- Generic Name
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
- Model / Reference
- DIS-KCUP-254 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840050505779 FDA UDI
- 510(k) Number
- K180349 FDA UDI
- FDA Product Code
- PTH FDA UDINFT FDA UDINGL FDA UDIQAW FDA UDINFY FDA UDIPTG FDA UDINFV FDA UDINGM FDA UDINGG FDA UDIQBF FDA UDINFW FDA UDI
- GMDN Term
- Multiple drugs of abuse IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3150 FDA UDI862.3100 FDA UDI862.3650 FDA UDI862.3910 FDA UDI862.3250 FDA UDI862.3620 FDA UDI862.3170 FDA UDI862.3610 FDA UDI862.3700 FDA UDI862.3870 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: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Discover by American Screening, L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K180349 also covers:
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
- Discover Plus — AMERICAN SCREENING, L.L.C.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- American Screening, L.l.c.
Sources (1)
- FDA UDI c7871d38-d603-47df-95f5-4e8cc6c03642 33 fields · synced May 30, 2026