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490101

by Intuitive Surgical, Inc.

Ref 490101

490101 is a device classified as Class IIa in the EU and Class II in the US made by Intuitive Surgical, Inc., registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 088687412267999) and listed in FDA GUDID since 5 Sep 2019 (UDI-DI 00886874119846), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number088687412267999 Basic UDI-DI 00886874119846UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00886874119846 UDI-DI Date5 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 088687412267999 registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 00886874119846 listed 5 Sep 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00886874119846
  2. Registered EUDAMED 088687412267999

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  • Withdrawn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

Trade name
Vision Probe Adapter and Suction Adapter
Generic name
Luminal device flushing tubing set, single-use
Device name
Ion Adapters
Model / reference
490101
Primary DI / UDI-DI
00886874119846
Basic UDI-DI
088687412267999
FDA product code
EOQ
EMDN code
Z12020885 Pulmonary endoscopic instruments - consumables
GMDN term
Luminal device flushing tubing set, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
874.4680
EU registration type
Standard device
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 II

Device class is stated on each registry's own scale: Class IIa 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: Luminal device flushing tubing set, single-use

Similar devices in this category

Other devices filed under PULMONARY ENDOSCOPIC INSTRUMENTS.

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (19, all answered No)