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Planmeca Olo

by Planmeca Oy

Ref 10033200

Planmeca Olo (10033200) is a Class I device made by Planmeca Oy, registered in EUDAMED on 1 Dec 2021 (Basic UDI-DI 6430035420025F), 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 Number6430035420025F Basic UDI-DI 06430035420537UDI-DIDate1 Dec 2021RegisteredStatusActive

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  • Withdrawn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
Planmeca Olo
Model / reference
10033200
Primary DI / UDI-DI
06430035420537
Basic UDI-DI
6430035420025F
EMDN code
Z11030380 Instruments for extraoral dental radiology - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000006499

Similar devices in this category

Other devices filed under INSTRUMENTS FOR EXTRAORAL DENTAL RADIOLOGY.

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Properties

Other properties (14, all answered No)