Identity
- Trade Name
- Ethyl Alcohol ETH FDA UDI
- Generic Name
- Ethanol (ETOH) IVD, kit, enzyme spectrophotometry FDA UDI
- Model / Reference
- 11868152190 FDA UDI
Identifiers
- Catalog Number
- 11868152190 FDA UDI
- Primary DI / UDI-DI
- 04015630991778 FDA UDI
- 510(k) Number
- K952839 FDA UDI
- FDA Product Code
- DML FDA UDI
- GMDN Term
- Ethanol (ETOH) IVD, kit, enzyme spectrophotometry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3040 FDA UDI
- Commercial Distribution
- Not 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
Ethyl Alcohol ETH by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K952839 also covers:
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
- Roche Diagnostics Corp.
Sources (1)
- FDA UDI d0681570-7154-4b27-b35f-8512f37e9610 36 fields · synced May 30, 2026