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Intense Pulsed Light Equipment

by Beijing Globalipl Development Co., Ltd 3 variants

Ref US301

Intense Pulsed Light Equipment (US301) is a medical device (EU MDR Class IIb; EMDN category multi–platform laser) made by Beijing Globalipl Development Co., Ltd., registered in EUDAMED on 29 Sep 2026 (Basic UDI-DI 697349493US3Y2), active as of 25 Oct 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697349493US3Y2 Basic UDI-DI 06973494930099UDI-DIDate29 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
US301
Primary DI / UDI-DI
06973494930099
Basic UDI-DI
697349493US3Y2
Direct marketing DI
06973494930099
EMDN code
Z12011019 Multi–platform laser
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000010924
Authorised representative
MedNet EC-REP C IIb GmbH DE-AR-000011194

Similar devices in this category

Other devices filed under MULTI–PLATFORM LASER.

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Properties

  • Reusable
Other properties (13, all answered No)