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Conmed 0037060

by Conmed Corporation

Ref 0037060

Conmed 0037060 is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 27 Apr 2026 (Basic UDI-DI B-10653405000594) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10653405000594), active as of 23 Oct 2026.

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

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10653405000594 Basic UDI-DI 10653405000594UDI-DIDate27 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405000594 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10653405000594 registered 27 Apr 2026 Active
  • FDA GUDID UDI-DI 10653405000594 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10653405000594
  2. Registered EUDAMED B-10653405000594

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Conmed
Generic name
Suction/irrigation tubing, single-use
Device name
Non-orthopedic, Non-active, Accessory, Tubing/Connector, Suction, Sterile
Model / Ref / Catalog
0037060
Primary DI / UDI-DI
10653405000594
Basic UDI-DI
B-10653405000594
FDA product code
BYY
EMDN code
A070101 Suction tubing adapters and connectors
GMDN term
Suction/irrigation tubing, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Length — 3.7 Meter
Length — 12 Feet

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 10653405000594: EUDAMED states No, FDA GUDID states Yes.

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: Suction/irrigation tubing, single-use

Similar devices in this category

Other devices filed under ADAPTERS AND CONNECTORS.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)