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Astar

by Astar Orthodontics Inc. 4 variants

Ref 5268-5004Model Middle, Orange

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-5268-5004NA Basic UDI-DI D-5268-5004NAUDI-DIDate14 Nov 2022RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Reverse Pull Headgear(Face Mask)
Model / Reference
Middle, Orange, 5268-5004
Primary DI / UDI-DI
D-5268-5004NA
Basic UDI-DI
B-5268-5004NA
EMDN Code
Q010401 Orthodontic face bows
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000028647
Authorised representative
BIO CONCEPT, UNIPESSOAL, LDA PT-AR-000021480

Other devices from Astar Orthodontics Inc.

See all devices from Astar Orthodontics Inc. →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No