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Cable Assembly, USB ADC to Philips #C01 BP Module

EUDAMEDFDA UDI

Class I (EU MDR)

Ref LI11063

by LiDCO Ltd

Identity

Trade Name
Cable Assembly, USB ADC to Philips #C01 BP Module EUDAMED
LiDCO Ltd FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Cable Assembly, USB ADC to Philips #C01 BP Module EUDAMEDFDA UDI
Model / Reference
LI11063 EUDAMEDFDA UDI
Description
Cable Assembly, USB ADC to Philips #C01 BP Module FDA UDI

Identifiers

Catalog Number
Li11063 FDA UDI
Primary DI / UDI-DI
05060110522231 EUDAMEDFDA UDI
Basic UDI-DI
506011052000Z7T0C01V0019N EUDAMED
510(k) Number
K163334 FDA UDI
FDA Product Code
DXG FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.1435 FDA UDI
Market of Registration
Denmark 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

Category: Device sterilization/disinfection container, reusable

Cable Assembly, USB ADC to Philips #C01 BP Module by LiDCO Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LiDCO Ltd
EUDAMED SRN
GB-MF-000008036
Authorised Representative
LiDCO Netherlands B.V. NL-AR-000002681

Sources (2)

  • EUDAMED b08aba5f-6f7d-47e9-817f-4e0f0ccf912b 61 fields · synced Jul 11, 2026
  • FDA UDI a93d06d0-e9b5-47c9-9631-a03be9d12802 36 fields · synced May 30, 2026