← Back to catalogue
CNAP Arm Cuff
EUDAMEDFDA UDIClass I (EU MDR)
Ref Li10717Model Li10716
by LiDCO Ltd
Identity
- Trade Name
- CNAP Arm Cuff EUDAMEDLiDCO Ltd FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- CNAP Arm Cuff, Child, Range 12-19cm EUDAMEDCNAP Arm Cuff, Small Adult, Range 17-25cm FDA UDI
- Model / Reference
- Li10716 EUDAMEDLi10717 EUDAMEDFDA UDI
- Description
- CNAP Arm Cuff, Small Adult, Range 17-25cm FDA UDI
Identifiers
- Catalog Number
- Li10717 FDA UDI
- Primary DI / UDI-DI
- 05060110521197 EUDAMEDFDA UDI
- Basic UDI-DI
- 506011052000Z7T7C01V000DR EUDAMED
- 510(k) Number
- K131048 FDA UDI
- FDA Product Code
- DXG FDA UDI
- EMDN Code
- Z1203020501 NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGES EUDAMED
- GMDN Term
- General-purpose multi-parameter bedside monitor FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1435 FDA UDI
- Market of Registration
- Czechia EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
CNAP Arm Cuff by LiDCO Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 506011052000Z7T7C01V000DR | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- LiDCO Ltd
- EUDAMED SRN
- GB-MF-000008036
- Authorised Representative
- LiDCO Netherlands B.V. NL-AR-000002681
Sources (2)
- EUDAMED fde2d932-8f18-4aa7-a57c-6be80150659e 61 fields · synced Jun 20, 2026
- FDA UDI 03b8623c-aa21-435c-a79d-71e2c90cb9ac 36 fields · synced May 30, 2026