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Y1500512

by Nakanishi Inc.

Part of a family of 11 devices: see the family page

Ref Y1500512Model SPP0000000

Y1500512 is a Class IIa device made by Nakanishi Inc., registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI 456022499000000074), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number456022499000000074 Basic UDI-DI 04589551396382UDI-DIDate29 Apr 2026RegisteredStatusActive EUDAMED: not on the EU market

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
SPP0000000, Y1500512
Primary DI / UDI-DI
04589551396382
Basic UDI-DI
456022499000000074
EMDN code
Q0199, Z12110102, Z12110180
Device class
Class IIa
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
Dental Treatment

Manufacturer details

EUDAMED SRN
JP-PR-000047454

Similar devices in this category

Other devices filed under INSTRUMENTS FOR DENTAL TREATMENT UNITS.

Other devices from Nakanishi Inc.

See all devices from Nakanishi Inc. →

Properties

  • Sterilise before use
Other properties (1, all answered No)