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Micro Instrument Co.

by Micro Instrument Co. 18 variants

Ref VERTEX- ENT

Active European Union

CE MDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8908019835VERTEX-ENTDE Basic UDI-DI 89080198351686UDI-DIDate27 Sep 2026RegisteredStatusActive

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  • Withdrawn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
Surgical Microscope
Model / Reference
VERTEX- ENT
Primary DI / UDI-DI
89080198351686
Basic UDI-DI
8908019835VERTEX-ENTDE
Direct Marketing DI
89080198351686
EMDN Code
Z12011101 Operative microscopes
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
IN-MF-000045953
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Micro Instrument Co.

See all devices from Micro Instrument Co. →

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