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470056

by Intuitive Surgical, Inc.

Ref 470056

470056 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 26 Oct 2026 (Basic UDI-DI 08868741199219X) and listed in FDA GUDID since 11 Nov 2019 (UDI-DI 00886874116562), 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 Number08868741199219X Basic UDI-DI 00886874116562UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00886874116562 UDI-DI Date11 Nov 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08868741199219X registered 26 Oct 2026 Active
  • FDA GUDID UDI-DI 00886874116562 listed 11 Nov 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00886874116562
  2. Registered EUDAMED 08868741199219X

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  • Withdrawn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
8 mm Endoscope Plus, 0°
Generic name
Rigid optical laparoscope
Device name
Endoscopes
Model / reference
470056
Primary DI / UDI-DI
00886874116562
Basic UDI-DI
08868741199219X
Direct marketing DI
00886874116562
FDA product code
NAY, GCJ
EMDN code
Z12029016 Video laparoscopes
GMDN term
Rigid optical laparoscope
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Hydrogen Peroxide
Size
Outer Diameter — 8 Millimeter
Angle — 0 degree

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: Rigid optical laparoscope

Similar devices in this category

Other devices filed under VIDEO LAPAROSCOPES.

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)