3D Roadmap 001003

GUDID 00884838059221

Software medical device, used with a Philips Interventional X-Ray System. Extension of 3D-RA. Superimposes live fluoroscopic images on a 3D reconstruction of the vessel anatomy.

Philips Medical Systems Nederland B.V.

Angiographic x-ray system application software
Primary Device ID00884838059221
NIH Device Record Keyc6cfea1c-dbf1-4429-a4c9-24278d839bea
Commercial Distribution StatusIn Commercial Distribution
Brand Name3D Roadmap
Version Model Number3D Roadmap R1
Catalog Number001003
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
GS100884838059221 [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 Number6
Public Version Date2019-10-24
Device Publish Date2016-09-24

Devices Manufactured by Philips Medical Systems Nederland B.V.

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00884838119277 - Philips Sentinelle2024-12-25 dS 1.5T Interface Box
00884838119284 - Philips Sentinelle2024-12-25 dS 3.0T Interface Box
00884838119291 - Philips Sentinelle2024-12-25 dS 1.5T 8CH Medial
00884838119307 - Philips Sentinelle2024-12-25 dS 3.0T 8CH Medial
00884838119314 - Philips Sentinelle2024-12-25 dS 1.5T 4CH Lateral Left
00884838119321 - Philips Sentinelle2024-12-25 dS 3.0T 4CH Lateral Left
00884838119338 - Philips Sentinelle2024-12-25 dS 1.5T 4CH Lateral Right

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