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Conmed 0048260

by Conmed Corporation

Ref 0048260

Conmed 0048260 is a device classified as Class I in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-20653405000737) and listed in FDA GUDID since 26 Jul 2021 (UDI-DI 20653405000737), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-20653405000737 Basic UDI-DI 20653405000737UDI-DIDate29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20653405000737 UDI-DI Date26 Jul 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-20653405000737 registered 29 Apr 2026 Active
  • FDA GUDID UDI-DI 20653405000737 listed 26 Jul 2021 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 20653405000737
  2. Registered EUDAMED B-20653405000737

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  • Withdrawn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, Non-sterile
Model / Ref / Catalog
0048260
Primary DI / UDI-DI
20653405000737
Basic UDI-DI
B-20653405000737
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

Truth per registry

2 sources · 2 fields differ

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

Registry differences

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

  • Sterilise before use UDI-DI 20653405000737: EUDAMED states Yes, FDA GUDID states No.

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

  • Sterilise before use YesEUDAMEDNoGUDID
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)