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 Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software Angiographic x-ray system application software

• Primary Device ID: 00884838059221
• NIH Device Record Key: c6cfea1c-dbf1-4429-a4c9-24278d839bea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3D Roadmap
• Version Model Number: 3D Roadmap R1
• Catalog Number: 001003
• Company DUNS: 413819707
• Company Name: Philips Medical Systems Nederland B.V.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838059221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121772

FDA Product Code

• OWB: Interventional Fluoroscopic X-Ray System

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-10-24
• Device Publish Date: 2016-09-24

Devices Manufactured by Philips Medical Systems Nederland B.V.

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• 00884838099210 - Azurion: 2023-09-26 Monoplane Interventional X-Ray System. A floor-mounted monoplane system with a 15-inch flat detector.