FDA UDI Not in Commercial Distribution 🇺🇸 United States

Allura Xper FD

DI: 00884838083448 · Model: Allura Xper R9 7 M20 · Philips Medical Systems Nederland B.V.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Allura Xper FD
Primary DI
00884838083448
Version / Model
Allura Xper R9 7 M20
Catalog Number
722066
Company Name
Philips Medical Systems Nederland B.V.
Labeler DUNS
413819707
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-31
Public Version
6
Public Version Date
2023-09-26
Public Version Status
Update
Public Device Record Key
08bc8eda-f108-406b-ba2f-890351ca3a97
Distribution End Date
2019-09-06

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 00884838083448

Premarket Submissions

Submission Number Supplement Number
K163715 000
K172822 000