Skip to content

DR Protector XL

by Philips Medical Systems DMC GmbH

Part of a family of 17 devices: see the family page

Ref 300013026841

DR Protector XL (300013026841) is a Class I device made by Philips Medical Systems DMC GmbH, registered in EUDAMED on 13 Dec 2024 (Basic UDI-DI 0884838BM448TA), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0884838BM448TA Basic UDI-DI 00884838126688UDI-DIDate13 Dec 2024RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Detector Accessory
Model / reference
300013026841
Primary DI / UDI-DI
00884838126688
Basic UDI-DI
0884838BM448TA
EMDN code
Z11039080 Various radiodiagnostic and interventional instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
DE-MF-000005362

Similar devices in this category

Other devices filed under VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Philips Medical Systems DMC GmbH

See all devices from Philips Medical Systems DMC GmbH →

Properties

Other properties (14, all answered No)