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inspired™ 2096534-003

by Vincent Medical Manufacturing Co., Limited

Ref 2096534-003

inspired 2096534-003 is an anaesthesia breathing circuit (EU MDD Class IIa; FDA Class I; FDA product code CAI, Circuit, Breathing (W Connector, Adaptor, Y Piece)) made by Vincent Medical Manufacturing Co., Limited, registered in EUDAMED on 29 May 2026 (Basic UDI-DI B-14896138001049) and listed in FDA GUDID since 18 Sep 2020 (UDI-DI 14896138001049), 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-14896138001049 Basic UDI-DI 14896138001049UDI-DIDate29 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14896138001049 UDI-DI Date18 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-14896138001049 registered 29 May 2026 Active
  • FDA GUDID UDI-DI 14896138001049 listed 18 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 14896138001049
  2. Registered EUDAMED B-14896138001049

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  • Withdrawn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
inspired™
Generic name
Anaesthesia breathing circuit, reusable
Model / reference
2096534-003
Primary DI / UDI-DI
14896138001049
Basic UDI-DI
B-14896138001049
FDA product code
CAI
EMDN code
R020199 Breathing circuits and kits - other
GMDN term
Anaesthesia breathing circuit, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
868.5240
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

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

Related devices

Category: Anaesthesia breathing circuit, reusable

Similar devices in this category

Other devices filed under BREATHING CIRCUITS AND KITS - OTHER.

Other devices from Vincent Medical Manufacturing Co., Limited

See all devices from Vincent Medical Manufacturing Co., Limited →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)