daVinci Si

GUDID 00886874110775

PATIENT SIDE CART, RECERTIFIED

INTUITIVE SURGICAL, INC.

Robotic surgical system
Primary Device ID00886874110775
NIH Device Record Keyf915cb4b-16c7-4c62-a1ff-4443160136a5
Commercial Distribution StatusIn Commercial Distribution
Brand NamedaVinci Si
Version Model Number380686
Company DUNS938647021
Company NameINTUITIVE SURGICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100886874110775 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NAYSystem,surgical,computer controlled instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number7
Public Version Date2020-03-02
Device Publish Date2016-07-08

On-Brand Devices [daVinci Si]

00886874110881FLUORESCENCE IMAGING CAMERA HEAD AND CABLE KIT
00886874110874VISION SIDE SYSTEM
00886874110799VISION SIDE SYSTEM, RECERTIFIED
00886874110782SURGEON SIDE CONSOLE, RECERTIFIED
00886874110775PATIENT SIDE CART, RECERTIFIED
00886874110751PATIENT SIDE CART, RECERTIFIED
00886874110737PATIENT SIDE CART, 4-ARM, RECERTIFIED
00886874110713PATIENT SIDE CART, 3-ARM
00886874110690PATIENT SIDE CART, 4-ARM
00886874110683SURGEON SIDE CONSOLE

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