Identity
- Trade Name
- LiDCO Ltd FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- CNAP Cuff Controller Fixation Strap FDA UDI
- Model / Reference
- Li10712 FDA UDI
- Description
- CNAP Cuff Controller Fixation Strap FDA UDI
Identifiers
- Catalog Number
- Li10712 FDA UDI
- Primary DI / UDI-DI
- 05060110521159 FDA UDI
- 510(k) Number
- K131048 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
- 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose multi-parameter bedside monitor
LiDCO Ltd by Lidco Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose multi-parameter bedside monitor.
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- Expression MR200 Accessories — Philips DS North America LLC · Class II
- IBP Adapter Cable — Orantech Inc. · Class I
- HemoSphere Alta — Edwards Lifesciences LLC · Class II
- VitaLogik4500 — Mennen Medical, Inc. · Class II
Cleared under the same submission
K131048 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 60f3cdf7-b141-40d0-b4a5-2c5aad488f76 36 fields · synced May 30, 2026