FDA UDI In Commercial Distribution 🇺🇸 United States

LF

DI: 10746190002871 · Model: 814004 · Liebel-Flarsheim Company LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LF
Primary DI
10746190002871
Version / Model
814004
Company Name
Liebel-Flarsheim Company LLC
Labeler DUNS
080186051
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-29
Public Version
4
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
a0777d4a-bc32-40cd-8713-0e6c2eceeb09

Device Description

OptiStar Elite MR Contrast Delivery System

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 Conditional
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
DXT Injector And Syringe, Angiographic

GMDN Terms

Code Name
58002 MRI contrast medium injection system, line-powered, stationary

Identifiers

Type ID
Primary 10746190002871

Premarket Submissions

Submission Number Supplement Number
K073592 000