FDA UDI In Commercial Distribution 🇺🇸 United States

SmartCT

DI: 00884838085732 · Model: SmartCT - 1 · Philips Medical Systems Nederland B.V.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SmartCT
Primary DI
00884838085732
Version / Model
SmartCT - 1
Catalog Number
001018
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
2021-02-25
Public Version
2
Public Version Date
2023-09-26
Public Version Status
Update
Public Device Record Key
451182ea-a676-4b08-bbb3-9f68d6156014

Device Description

Software medical device, used with a Philips Interventional X-Ray System. Assists physicians by providing 3D views of the anatomy combined with planning and life guidance functionality.

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
JAK System, X-Ray, Tomography, Computed
LLZ System, Image Processing, Radiological

GMDN Terms

Code Name
40868 Angiographic x-ray system application software

Identifiers

Type ID
Primary 00884838085732

Premarket Submissions

Submission Number Supplement Number
K201583 000