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333 Monitor Suspension Systems

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 333/1/510/0031

by Kenex (Electro-Medical) Limited

Identity

Trade Name
333 Monitor Suspension Systems EUDAMED
KENEX FDA UDI
Generic Name
Medical monitor/light mount FDA UDI
Device Name
Pendant Systems for monitor and controls EUDAMED
333/1/510/0031 5-10kg Monitor system plus 250cm ceiling track FDA UDI
Model / Reference
333/1/510/0031 EUDAMEDFDA UDI
Description
333/1/510/0031 5-10kg Monitor system plus 250cm ceiling track FDA UDI

Identifiers

Catalog Number
333/1/510/0031 FDA UDI
Primary DI / UDI-DI
05055449407601 EUDAMEDFDA UDI
Basic UDI-DI
50554494PDOWU EUDAMED
FDA Product Code
FSY FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Medical monitor/light mount FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
878.4580 FDA UDI
Market of Registration
Northern Ireland 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Device sterilization/disinfection container, reusable

333 Monitor Suspension Systems by Kenex (electro-Medical) Limited — 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

EUDAMED SRN
GB-MF-000009022
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED bd6ebfd6-fb6c-406e-a12d-53fb3c42759e 61 fields · synced Oct 7, 2026
  • FDA UDI f19e5157-403f-434a-b7df-6e2b3067d30a 34 fields · synced May 30, 2026