FDA UDI In Commercial Distribution 🇺🇸 United States

Azurion

DI: 00884838116757 · Model: Azurion 5 M20 · 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
00884838116757
Version / Model
Azurion 5 M20
Catalog Number
722232
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
2023-08-31
Public Version
2
Public Version Date
2023-09-26
Public Version Status
Update
Public Device Record Key
6e7670f4-15f5-4c10-ae62-fedde6aa4b08

Device Description

Monoplane Interventional X-Ray System. A ceiling or floor-mounted monoplane system with a 20-inch flat detector.

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
JAA System, x-ray, fluoroscopic, image-intensified
OWB Interventional fluoroscopic x-ray system

GMDN Terms

Code Name
37623 Stationary angiographic x-ray system, digital

Identifiers

Type ID
Primary 00884838116757

Premarket Submissions

Submission Number Supplement Number
K200917 000

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 110 KiloPascal
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-13 – 158 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius