Identity
- Trade Name
- LiDCO FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- * INACTIVE Software Upgrade, LiDCOunity v2.03 (b301) FDA UDI
- Model / Reference
- Li11178 FDA UDI
- Description
- * INACTIVE Software Upgrade, LiDCOunity v2.03 (b301) FDA UDI
Identifiers
- Catalog Number
- Li11178 FDA UDI
- Primary DI / UDI-DI
- 05060110522767 FDA UDI
- 510(k) Number
- K163334 FDA UDI
- FDA Product Code
- DXG FDA UDI
- GMDN Term
- General-purpose multi-parameter bedside monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1435 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
LiDCO by Lidco Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K163334 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
- Lidco Limited
Sources (1)
- FDA UDI 849f80a6-4cd4-47c0-838f-1781a297ac84 37 fields · synced Jun 1, 2026