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Name: Spektra Model: Nickel Titanium arches

by Micerium S.p.A. EUDAMED

Active European Union

Ref ASNA20LModel Nickel Titanium

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++EMICFAM3A1ANTHC Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

Italy
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 1 country, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Italy since 5 Dec 2024

Last checked 27 Oct 2026.

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Name: Spektra Model: Nickel Titanium arches
Model / Reference
Nickel Titanium, ASNA20L
Primary DI / UDI-DI
EMICASNA20L1
Basic UDI-DI
++EMICFAM3A1ANTHC
EMDN Code
Q010401 Orthodontic face bows
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000010187

Other devices from Micerium S.p.A.

See all devices from Micerium S.p.A. →

Properties

Other properties (13)

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