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Ion 490206

by Intuitive Surgical, Inc.

Ref 490206

Ion 490206 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 08868741211227C) and listed in FDA GUDID since 6 May 2021 (UDI-DI 00886874121184), 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 Number08868741211227C Basic UDI-DI 00886874121184UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00886874121184 UDI-DI Date6 May 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08868741211227C registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 00886874121184 listed 6 May 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00886874121184
  2. Registered EUDAMED 08868741211227C

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  • Withdrawn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
Peripheral Vision Probe EUDAMED
Ion GUDID
Generic name
Flexible video bronchoscope, single-use
Device name
Ion Vision Probe
Model / reference
490206
Primary DI / UDI-DI
00886874121184
Basic UDI-DI
08868741211227C
Direct marketing DI
00886874121184
FDA product code
EOQ
EMDN code
Z12020802 Video bronchoscopes
GMDN term
Flexible video bronchoscope, 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: Flexible video bronchoscope, single-use

Similar devices in this category

Other devices filed under VIDEO BRONCHOSCOPES.

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

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