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T-connector

by Serres Oy

Ref 570610, 576109, 57610

T-connector (570610) is a suction system canister liner (EU MDR Class I; FDA Class II; FDA product code KDQ, Bottle, Collection, Vacuum) made by Serres Oy, registered in EUDAMED on 4 Feb 2022 (Basic UDI-DI 6418685SBS37U) and listed in FDA GUDID since 14 Sep 2026 (UDI-DI 06418685062758), active as of 22 Oct 2026.

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

CE MDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06418685062758 UDI-DI Date14 Sep 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number6418685SBS37U Basic UDI-DI Date4 Feb 2022RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 6418685SBS37U registered 4 Feb 2022 Active
  • FDA GUDID UDI-DI 06418685062758 listed 14 Sep 2026 Listed

Timeline

2 dated events

  1. Registered EUDAMED 6418685SBS37U
  2. Listed FDA GUDID 06418685062758

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  • Withdrawn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
Suction system canister liner
Model / reference
570610, 576109, 57610
Primary DI / UDI-DI
06418685062758 EUDAMED
06418685062093 EUDAMED
06418685021427 EUDAMED
06418685050410 GUDID
Basic UDI-DI
6418685SBS37U
FDA product code
KDQ
EMDN code
A070199 Adapters and connectors - other
GMDN term
Suction system canister liner
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Standard device
EU market of registration
Finland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
06418685062758
06418685062093
06418685021427
GUDID
06418685050410
Device classEUDAMED
Class I
GUDID
Class II

The registries describe this device under different primary UDI-DIs (EUDAMED lists 06418685062758, 06418685062093, 06418685021427; FDA GUDID lists 06418685050410), so their flags are not compared. 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.

Manufacturer details

EUDAMED SRN
FI-MF-000004504

Similar devices in this category

Other devices filed under ADAPTERS AND CONNECTORS - OTHER.

Other devices from Serres Oy

See all devices from Serres Oy →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)