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Planmeca Emerald

by Planmeca Oy

Ref 30006359

Planmeca Emerald (30006359) is a Class I device made by Planmeca Oy, registered in EUDAMED on 21 Apr 2022 (Basic UDI-DI 6430035420035H), 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 Number6430035420035H Basic UDI-DI 06430035420568UDI-DIDate21 Apr 2022RegisteredStatusActive

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  • Withdrawn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 Emerald
Model / reference
30006359
Primary DI / UDI-DI
06430035420568
Basic UDI-DI
6430035420035H
EMDN code
Z110601 Laser imaging scanner
Device class
Class I
EU registration type
Standard device
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000006499

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Properties

Other properties (14, all answered No)