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Minop®

by Schölly Fiberoptic GmbH 3 variants

Ref PE540AModel Neuroscopes

Minop® (PE540A) is a Class III device made by SCHÖLLY FIBEROPTIC GmbH, registered in EUDAMED on 29 May 2026 (Basic UDI-DI 42504801NEUROSCOPESY5) with CE/MDR certificate 1000285837 valid until 27 Apr 2027, active as of 24 Oct 2026.

Expiring European Union

CE MDR

Valid until

27 Apr 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42504801NEUROSCOPESY5 Basic UDI-DI 04250480103418UDI-DIDate29 May 2026RegisteredStatusActive

Official records

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 1000276655 Active

    Technical documentation EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    11 Dec 2025
    Expires
    10 Dec 2030
  • 1000285837 Restricted

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    15 Jan 2026
    Expires
    27 Apr 2027
    Reason
    Not on market

Timeline

5 dated events

  1. Certificate issued EUDAMED 1000276655
  2. Certificate issued EUDAMED 1000285837
  3. Registered EUDAMED 42504801NEUROSCOPESY5
  4. Certificate expires EUDAMED 1000285837
  5. Certificate expires EUDAMED 1000276655

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Expiring

Specification

EUDAMED

Model / reference
Neuroscopes, PE540A
Primary DI / UDI-DI
04250480103418
Basic UDI-DI
42504801NEUROSCOPESY5
Direct marketing DI
04250480103418
EMDN code
Z12020902 Neuroscopes
Device class
Class III
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005618

Similar devices in this category

Other devices filed under NEUROENDOSCOPY INSTRUMENTS.

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See all devices from SCHÖLLY FIBEROPTIC GmbH →

Properties

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