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daVinci Si 380681

by Intuitive Surgical, Inc.

daVinci Si 380681 is a Class II device made by Intuitive Surgical, Inc., listed in FDA GUDID since 8 Jul 2016 (UDI-DI 00886874110751), 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 Number00886874110751 UDI-DI Date8 Jul 2016ListedStatusListed 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  • Withdrawn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

Trade name
daVinci Si
Generic name
Robotic surgical telemanipulation system
Model / reference
380681
Primary DI / UDI-DI
00886874110751
FDA product code
NAY
GMDN term
Robotic surgical telemanipulation system
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Robotic surgical arm system

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Other devices filed under Robotic surgical arm system.

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Properties

  • Sterilise before use
  • Prescription use
  • Serial number
Other properties (12, all answered No)