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Cimpax

by Conmed Corporation

Ref C32-10-002, C32-01-750, C32-25-001

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number084585408507DB Basic UDI-DI Date11 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number30845854081710 UDI-DI Date30 Sep 2020ListedStatusListed GUDID: in commercial distribution

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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Electrical-only medical device connection cable, reusable
Surgical plume evacuation system
Surgical plume evacuation system filter
Device Name
Non-orthopedic, Non-active, Accessory, Cable/Cord
Non-orthopedic, Active, Smoke Evacuation Unit, ViroVac
Non-orthopedic, Non-active, Smoke Evacuation Filter
Model / Ref / Catalog
C32-10-002, C32-01-750, C32-25-001
Primary DI / UDI-DI
30845854081710, 30845854081734, 30845854081727
Basic UDI-DI
084585408507DB, 084585408469DU, 084585408515DA
510(k) Number
FDA Product Code
FYD
EMDN Code
L0317, Z12019004
GMDN Term
Electrical-only medical device connection cable, reusable
Surgical plume evacuation system
Surgical plume evacuation system filter
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
878.5070
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription Use
  • Lot / Batch Number YesGUDIDNoGUDID
  • Serial Number NoGUDIDYesGUDID
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No