FDA UDI In Commercial Distribution 🇺🇸 United States

MEDRAD® Stellant FLEX CT Injection System with Certegra® Workstation (Upgrade)

DI: 00616258020792 · Model: Stellant FLEX · BAYER MEDICAL CARE INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MEDRAD® Stellant FLEX CT Injection System with Certegra® Workstation (Upgrade)
Primary DI
00616258020792
Version / Model
Stellant FLEX
Catalog Number
FLEX UPG
Company Name
BAYER MEDICAL CARE INC.
Labeler DUNS
058716649
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-22
Public Version
1
Public Version Date
2018-12-24
Public Version Status
New
Public Device Record Key
ae8b8c5e-1809-401f-9f6c-3bbf9f49f575

Device Description

SYSTEM,DUAL,STELLANT,REMANUFACTURED,FLEX (85631829)

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IZQ Injector, Contrast Medium, Automatic
DXT Injector And Syringe, Angiographic

GMDN Terms

Code Name
57999 CT contrast medium injection system, line-powered, mobile

Identifiers

Type ID
Primary 00616258020792

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K173773 000