Skip to content

490115

by Intuitive Surgical, Inc. 2 variants

490115 is a Class II device made by Intuitive Surgical, Inc., listed in FDA GUDID since 21 Mar 2019 (UDI-DI 00886874119082), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886874119082 UDI-DI Date21 Mar 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Endoscope cleaning brush, reusable
Model / reference
490115
Primary DI / UDI-DI
00886874119082
FDA product code
EOQ
GMDN term
Endoscope cleaning brush, reusable
Device class
Class II
Regulation number
874.4680
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscope cleaning brush, reusable

Similar devices

Other devices filed under FDA product code EOQ (Bronchoscope (flexible or rigid)).

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)