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490024

by Intuitive Surgical, Inc.

Ref 490024

490024 is a device classified as Class I in the EU and Class II in the US made by Intuitive Surgical, Inc., registered in EUDAMED on 4 Jun 2026 (Basic UDI-DI 08868741227168N) and listed in FDA GUDID since 30 May 2019 (UDI-DI 00886874119129), 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
European UnionCE/MDR EUDAMED Number08868741227168N Basic UDI-DI 00886874119129UDI-DIDate4 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00886874119129 UDI-DI Date30 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08868741227168N registered 4 Jun 2026 Active
  • FDA GUDID UDI-DI 00886874119129 listed 30 May 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00886874119129
  2. Registered EUDAMED 08868741227168N

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  • Withdrawn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
Reprocessing Accessories Kit
Generic name
Surgical instrument/endoscope cleaning utensil, reusable
Device name
Reprocessing Kit
Model / reference
490024
Primary DI / UDI-DI
00886874119129
Basic UDI-DI
08868741227168N
FDA product code
EOQ
EMDN code
V9099 Various devices not included in other classes - other
GMDN term
Surgical instrument/endoscope cleaning utensil, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
874.4680
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
The reprocessing accessories kit are intended to support the reprocessing of the Fully Articulating Catheter and Peripheral Vision Probe.
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

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: Surgical instrument/endoscope cleaning utensil, reusable

Similar devices in this category

Other devices filed under VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER.

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

  • Convenience kit
  • Lot / batch number
Other properties (13, all answered No)