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Cheek retractors

by Larident SRL 8 variants

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

Ref A3-B

Cheek retractors (A3-B) is a Class I device made by Larident SRL, registered in EUDAMED on 22 Apr 2026 (Basic UDI-DI 8053504980ADEE), active as of 24 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8053504980ADEE Basic UDI-DI 08053504980332UDI-DIDate22 Apr 2026RegisteredStatusActive

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  • Withdrawn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
Apribocca in plastica sterilizzabile
Model / reference
A3-B
Primary DI / UDI-DI
08053504980332
Basic UDI-DI
8053504980ADEE
Direct marketing DI
08053504980332
EMDN code
L150201 Dental retractors, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007807

Similar devices in this category

Other devices filed under DENTAL RETRACTORS, REUSABLE.

Other devices from Larident SRL

See all devices from Larident SRL →

Properties

  • Sterilise before use
Other properties (13, all answered No)