XperGuide 001006

GUDID 00884838059252

Software medical device, used with a Philips Interventional X-Ray System. Extension of XperCT. Intended to assist the user during percutaneous interventions by providing live 3D needle image guidance.

Philips Medical Systems Nederland B.V.

Angiographic x-ray system application software
Primary Device ID00884838059252
NIH Device Record Key82093a8f-2ceb-48fa-bd2d-3689ccff270f
Commercial Distribution StatusIn Commercial Distribution
Brand NameXperGuide
Version Model NumberXperGuide R1
Catalog Number001006
Company DUNS413819707
Company NamePhilips Medical Systems Nederland B.V.
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 Batchtrue
Serial Numberfalse
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
GS100884838059252 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OWBInterventional Fluoroscopic X-Ray System

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number8
Public Version Date2019-12-02
Device Publish Date2016-09-24

Devices Manufactured by Philips Medical Systems Nederland B.V.

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