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Pax

EUDAMED

Class I (EU MDR)

Ref PML30(Wall-mount)Model PX401、PX402、PX403、PX405、PX407、PX408、PX409、PX411、PX413、PX414、PML30、PML30K、LED-F4/F4、LED-F4/F3、LED-F3/F3、LED-F4、LED-F3、PD160/160、PD160/120、PD120/120、PD160、PD120

by Shanghai PAX Medical Instrument Co., Ltd.

Identity

Trade Name
PAX EUDAMED
Device Name
Operating Light EUDAMED
Model / Reference
PX401、PX402、PX403、PX405、PX407、PX408、PX409、PX411、PX413、PX414、PML30、PML30K、LED-F4/F4、LED-F4/F3、LED-F3/F3、LED-F4、LED-F3、PD160/160、PD160/120、PD120/120、PD160、PD120 EUDAMED
PML30(Wall-mount) EUDAMED

Identifiers

Primary DI / UDI-DI
06975678803076 EUDAMED
Basic UDI-DI
697567880OL002QZ EUDAMED
EMDN Code
Z12010701 FIXED SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Operating room light system

Pax by Shanghai PAX Medical Instrument Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000027540
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 0039aeed-f1f7-49a9-a6ed-6b76312ba56a 61 fields · synced Jul 31, 2026