FDA UDI In Commercial Distribution 🇺🇸 United States

Dynamic Coronary Roadmap

DI: 00884838101883 · Model: Dynamic Coronary Roadmap - 3 · Philips Medical Systems Nederland B.V.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dynamic Coronary Roadmap
Primary DI
00884838101883
Version / Model
Dynamic Coronary Roadmap - 3
Catalog Number
001016
Company Name
Philips Medical Systems Nederland B.V.
Labeler DUNS
413819707
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-10
Public Version
2
Public Version Date
2023-09-26
Public Version Status
Update
Public Device Record Key
3f4b1adf-7857-4f73-9534-8330f1d4595f

Device 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.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OWB Interventional Fluoroscopic X-Ray System
LLZ System, Image Processing, Radiological

GMDN Terms

Code Name
40868 Angiographic x-ray system application software

Identifiers

Type ID
Primary 00884838101883

Premarket Submissions

Submission Number Supplement Number
K170130 000
K172307 000