Manufacturers

INTUITIVE SURGICAL INC.

10 devices in the database

PRECISE BIPOLAR FORCEPS
  • Model / Serial
    Model Catalog: 400110 (Lot serial: M10120817); Model Catalog: 400110 (Lot serial: M10130304); Model Catalog: 400110 (Lot serial: M10130205); Model Catalog: 400110 (Lot serial: M10121206); Model Catalog: 400172 (Lot serial: M10120918); Model Catalog: 400172 (Lot serial: M10120831); Model Catalog: 400172 (Lot serial: M10121008)
  • Product Description
    Precise Bipolar Forceps 8mm
STAPLER
  • Model / Serial
    Model Catalog: 470298 (Lot serial: )
  • Product Description
    DA VINCI XI ENDOWRIST STAPLER RELEASE KIT (SRK)
DA VINCI SI SYSTEM - SURGEON CONSOLE
  • Model / Serial
    Model Catalog: SS3000 (Lot serial: SH2240); Model Catalog: SS3000 (Lot serial: SH1104); Model Catalog: SS3000 (Lot serial: SH0948)
  • Product Description
    DA VINCI SI (IS3000) SURGEON CONSOLE TOUCHPAD
DA VINCI SI SYSTEM - MAIN
  • Model / Serial
    Model Catalog: IS3000 (Lot serial: >10 serial numbers.); Model Catalog: IS3000 (Lot serial: Contact manufacturer.); Model Catalog: IS2000 (Lot serial: >10 serial numbers.); Model Catalog: IS2000 (Lot serial: contact manufacturer.)
  • Product Description
    Da Vinci SI System
DA VINCI SI SYSTEM - MAIN
  • Model / Serial
    Model Catalog: IS3000 (Lot serial: all lots. contact mfg); Model Catalog: IS1200 (Lot serial: all lots. contact mfg); Model Catalog: IS2000 (Lot serial: all lots. contact mfg)
  • Product Description
    Da Vinci Si System - Main
5 more

13 manufacturers with a similar name

Learn more about the data here

Intuitive Surgical Inc.
Intuitive Surgical Inc.
Intuitive Surgical Inc.
Intuitive Surgical Inc.
Intuitive Surgical Inc.
  • Manufacturer Parent Company (2017)
    Intuitive Surgical Inc
  • Manufacturer comment
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
8 more