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LiDCO Ltd

FDA UDI

Class II (US FDA UDI)

by Lidco Limited

Identity

Trade Name
LiDCO Ltd FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Device Name
Smartcard, Demo, LiDCOrapid, 600,000 Minutes,LiDCO Internal Use Only FDA UDI
Model / Reference
Li10529 FDA UDI
Description
Smartcard, Demo, LiDCOrapid, 600,000 Minutes,LiDCO Internal Use Only FDA UDI

Identifiers

Catalog Number
Li10529 FDA UDI
Primary DI / UDI-DI
05060110520343 FDA UDI
510(k) Number
K010049 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.

Cleared under the same submission

K010049 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lidco Limited

Sources (1)

  • FDA UDI a8442ed1-e8cc-4987-94a3-f2f9c9c29049 36 fields · synced May 30, 2026