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Pico Max

by Ids Ltd.

Ref IDS-UM-1031Model PICO MAX

Pico Max (IDS-UM-1031) is a medical device (EU MDD Class IIb; EMDN category neodymium surgical laser) made by Ids Ltd., registered in EUDAMED on 12 Mar 2026 (Basic UDI-DI B-08809578390306), active as of 22 Oct 2026.

Active European Union

CE MDD

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08809578390306 Basic UDI-DI 08809578390306UDI-DIDate12 Mar 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Picosecond Nd:YAG Laser
Model / reference
PICO MAX, IDS-UM-1031
Primary DI / UDI-DI
08809578390306
Basic UDI-DI
B-08809578390306
EMDN code
Z12011017 Neodymium surgical laser
Device class
Class IIb
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000018259
Authorised representative
Obelis s.a. BE-AR-000000106

Similar devices in this category

Other devices filed under NEODYMIUM SURGICAL LASER.

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Properties

Other properties (12, all answered No)