FDA UDI In Commercial Distribution 🇺🇸 United States

Azurion

DI: 00884838085367 · Model: Azurion 7 B20 · Philips Medical Systems Nederland B.V.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Azurion
Primary DI
00884838085367
Version / Model
Azurion 7 B20
Catalog Number
722068
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
2017-12-04
Public Version
6
Public Version Date
2023-09-26
Public Version Status
Update
Public Device Record Key
56efee75-4a8f-43c1-bbe6-cb7367eeb6d0

Device Description

Biplane Interventional X-Ray System with floor-mounted frontal stand (20-inch flat detector), ceiling-mounted lateral stand (12-inch or 15-inch flat detector) and optional interface for an OR table.

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
Yes
Has Lot/Batch Number
No
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00884838085367

Premarket Submissions

Submission Number Supplement Number
K172822 000