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Cable Assembly, LiDCO BP Module to Edwards Transducer

EUDAMEDFDA UDI

Class I (EU MDR)

Ref LI10611Model LI10610

by LiDCO Ltd

Identity

Trade Name
Cable Assembly, LiDCO BP Module to Edwards Transducer EUDAMED
LiDCO Ltd FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Cable Assembly, LiDCO BP Module to BD/Argon Transducer EUDAMED
Cable Assembly, LiDCO BP Module to Edwards Transducer FDA UDI
Model / Reference
LI10610 EUDAMED
LI10611 EUDAMEDFDA UDI
Description
Cable Assembly, LiDCO BP Module to Edwards Transducer FDA UDI

Identifiers

Catalog Number
Li10611 FDA UDI
Primary DI / UDI-DI
05060110520831 EUDAMEDFDA UDI
Basic UDI-DI
506011052000Z7T0C01V0049U EUDAMED
510(k) Number
K122247 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
Netherlands 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, LiDCO BP Module to Edwards Transducer 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 a4bcf444-a341-4c3b-8445-8311bb0fd2d4 61 fields · synced Jul 18, 2026
  • FDA UDI e2d1b9d5-78cf-4964-a9d0-a67f40a15cf3 36 fields · synced May 30, 2026