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Pax

EUDAMED

Class I (EU MDR)

Ref PAX-F700/500Model PANALEX-A、PANALEX-B、PANALEX-C、PANALEX-D、PANALEX-E、PANALEX 1、PANALEX 2、PANALEX 3、PANALEX 4、PANALEX 1(M)、PANALEX 1(W)、pax-XR1、pax-XR1 Pro、pax-XR1 Max、PAX-F700/700、PAX-F700/500、PAX-F700、PAX-F500

by Shanghai PAX Medical Instrument Co., Ltd.

Identity

Trade Name
PAX EUDAMED
Device Name
Operating Light EUDAMED
Model / Reference
PANALEX-A、PANALEX-B、PANALEX-C、PANALEX-D、PANALEX-E、PANALEX 1、PANALEX 2、PANALEX 3、PANALEX 4、PANALEX 1(M)、PANALEX 1(W)、pax-XR1、pax-XR1 Pro、pax-XR1 Max、PAX-F700/700、PAX-F700/500、PAX-F700、PAX-F500 EUDAMED
PAX-F700/500 EUDAMED

Identifiers

Primary DI / UDI-DI
06975678807142 EUDAMED
Basic UDI-DI
697567880OL001QX EUDAMED
EMDN Code
Z12010701 FIXED SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Romania 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 d0eddb6f-3c23-44b1-804d-ffa4e0c2fd3f 61 fields · synced Jun 19, 2026