Identity
- Trade Name
- A-dec FDA UDI
- Generic Name
- Medical device disinfection agent FDA UDI
- Device Name
- ICX Tablet,0.7 Liter,50 Count FDA UDI
- Model / Reference
- 90.1064.01 FDA UDI
- Description
- ICX Tablet,0.7 Liter,50 Count FDA UDI
Identifiers
- Catalog Number
- 90.1064.01 FDA UDI
- Primary DI / UDI-DI
- 10194665001339 FDA UDI
- 510(k) Number
- K051657 FDA UDI
- FDA Product Code
- LRJ FDA UDI
- GMDN Term
- Medical device disinfection agent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6890 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: Medical device disinfection agent
A-dec by A-Dec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K051657 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 I | Pending data |
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Manufacturer
- Manufacturer
- A-Dec, Inc.
Sources (1)
- FDA UDI 2e064ad6-c115-4932-945e-aba573ad3476 35 fields · synced Jun 8, 2026