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Dynamic Coronary Roadmap

FDA UDI

Class II (US FDA UDI)

by Philips Medical Systems Nederland B.V.

Identity

Trade Name
Dynamic Coronary Roadmap FDA UDI
Generic Name
Angiographic x-ray system application software FDA UDI
Device Name
Software medical device, used with a Philips Interventional X-Ray System. Intended to provide a real-time and dynamic angiographic roadmap of coronary arteries. FDA UDI
Model / Reference
Dynamic Coronary Roadmap - 1 FDA UDI
Description
Software medical device, used with a Philips Interventional X-Ray System. Intended to provide a real-time and dynamic angiographic roadmap of coronary arteries. FDA UDI

Identifiers

Catalog Number
001016 FDA UDI
Primary DI / UDI-DI
00884838080805 FDA UDI
510(k) Number
K170130 FDA UDI
FDA Product Code
OWB FDA UDI
LLZ FDA UDI
GMDN Term
Angiographic x-ray system application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 FDA UDI
892.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Angiographic x-ray system application software

Dynamic Coronary Roadmap by Philips Medical Systems Nederland B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic x-ray system application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 33e5758f-53da-45c7-b83c-6b3c1cf6ed05 35 fields · synced Sep 18, 2026