← Back to catalogue

Footrest 740

EUDAMED

Class I (EU MDR)

Ref 451220204331Ref 451220204332

by Philips Medical Systems DMC GmbH

Identity

Trade Name
Footrest 740 EUDAMED
Device Name
Foot rest EUDAMED
Model / Reference
451220204331 EUDAMED
451220204332 EUDAMED

Identifiers

Primary DI / UDI-DI
00884838098749 EUDAMED
00884838125902 EUDAMED
Basic UDI-DI
0884838BM444T2 EUDAMED
EMDN Code
Z11039080 VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Footrest 740 by Philips Medical Systems DMC GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005362

Sources (2)

  • EUDAMED 6b3d5a11-d94c-4f84-b4f3-69567c23cf89 61 fields · synced Oct 7, 2026
  • EUDAMED e89f5d31-1df3-46b0-893e-42ac596ef036 61 fields · synced May 17, 2026