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Diego Elite MDFS100

by Gyrus Acmi, Inc.

Ref MDFS100

Diego Elite MDFS100 is a device classified as Class I in the EU and Class II in the US made by Gyrus Acmi, Inc., registered in EUDAMED on 23 Jul 2026 (Basic UDI-DI 0821925000215B), cleared under FDA 510(k) K123429 on 5 Apr 2013 and listed in FDA GUDID since 14 Oct 2016 (UDI-DI 00821925027787), active as of 24 Oct 2026. 12 FDA recalls are linked to it.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None ongoing

12 closed

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K123429

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0821925000215B Basic UDI-DI 00821925027787UDI-DIDate23 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00821925027787 UDI-DI Date14 Oct 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK123429 Date5 Apr 2013DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 0821925000215B registered 23 Jul 2026 Active
  • FDA 510(k) K123429 decided 5 Apr 2013 Active
  • FDA GUDID UDI-DI 00821925027787 listed 14 Oct 2016 Listed

Recalls

12 recalls · FDA

  • 10 recalls, same reason

    • Terminated Z-1181-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1184-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1178-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1186-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1185-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1182-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1179-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1183-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1187-2019 FDA Class II initiated 8 Mar 2019
    • Terminated Z-1180-2019 FDA Class II initiated 8 Mar 2019

    Olympus Diego Elite Consoles may inadvertently permit activation of the RF energy feature when used with Diego Elite blades

  • 2 recalls, same reason

    • Terminated Z-1752-2015 FDA Class II initiated 8 May 2015
    • Terminated Z-1753-2015 FDA Class II initiated 8 May 2015

    Potential lack of sterility assurance.

Timeline

15 dated events

  1. Recall initiated FDA recalls Z-1184-2019
  2. Recall initiated FDA recalls Z-1178-2019
  3. Recall initiated FDA recalls Z-1186-2019
  4. Recall initiated FDA recalls Z-1185-2019
  5. Recall initiated FDA recalls Z-1182-2019
  6. Recall initiated FDA recalls Z-1179-2019
  7. Recall initiated FDA recalls Z-1183-2019
  8. Recall initiated FDA recalls Z-1187-2019
  9. Recall initiated FDA recalls Z-1180-2019
  10. Registered EUDAMED 0821925000215B

5 earlier events are in the sections above.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Diego Elite
Generic name
Electrosurgical system
Device name
ENT Microdebrider accessories
Model / reference
MDFS100
Primary DI / UDI-DI
00821925027787
Basic UDI-DI
0821925000215B
510(k) Number
FDA product code
GEI
EMDN code
Z12149080 Various ENT instruments - hardware accessories
GMDN term
Electrosurgical system
Device class
Class I EUDAMED
Class II GUDID
Regulation number
878.4400
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Electrosurgical system

Cleared under the same submission (K123429)

and 8 more cleared under K123429

Similar devices in this category

Other devices filed under VARIOUS ENT INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Gyrus Acmi, Inc.

See all devices from Gyrus Acmi, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)