2D Perfusion 001008

GUDID 00884838059276

Software medical device, used with a Philips Interventional X-Ray System. Provides a color coded representation of a digital subtraction angiography (DSA).

Philips Medical Systems Nederland B.V.

Angiographic x-ray system application software
Primary Device ID00884838059276
NIH Device Record Keyd0a2d1ed-02d0-40e9-a034-a71e05432202
Commercial Distribution StatusIn Commercial Distribution
Brand Name2D Perfusion
Version Model Number2D Perfusion R1
Catalog Number001008
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
GS100884838059276 [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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00884838128422 - Ingenia 2026-01-15 BlueSeal XE
00884838128439 - Ingenia 2026-01-15 MR 7700
00884838128446 - Ingenia 2026-01-15 MR 5300
00884838128453 - Ingenia 2026-01-15 Ingenia Elition S
00884838128460 - Ingenia 2026-01-15 Ingenia Elition X
00884838128477 - Ingenia, MR5300, MR7700, Achieva2026-01-15 Ingenia Ambition S
00884838128484 - Ingenia 3.0T2026-01-15 Ingenia Ambition X

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