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Micro Instrument Co.

by Micro Instrument Co. 18 variants

Ref Mi-7I00D

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8908019835Mi-7I00D77 Basic UDI-DI 89080198352126UDI-DIDate26 Sep 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
Indirect Ophthalmoscope
Model / Reference
Mi-7I00D
Primary DI / UDI-DI
89080198352126
Basic UDI-DI
8908019835Mi-7I00D77
EMDN Code
Z12120114 Ophthalmoscopes
Device Class
Class I

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