XperCT Dual 001105

GUDID 00884838059306

Software medical device, used with a Philips Interventional X-Ray System. Reconstructs 3D volumes from rotational fluoroscopic acquisitions and provides CT-like images to assist the physician.

Philips Medical Systems Nederland B.V.

Angiographic x-ray system application software
Primary Device ID00884838059306
NIH Device Record Keyccced8fd-0485-4734-8d55-37df01a9bce2
Commercial Distribution StatusIn Commercial Distribution
Brand NameXperCT Dual
Version Model NumberXperCT Dual R3
Catalog Number001105
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
GS100884838059306 [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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00884838128460 - Ingenia 2026-01-15 Ingenia Elition X
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00884838128484 - Ingenia 3.0T2026-01-15 Ingenia Ambition X

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