FDA UDI Not in Commercial Distribution 🇺🇸 United States

LF

DI: 10746190002017 · Model: 600172 · Liebel-Flarsheim Company LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LF
Primary DI
10746190002017
Version / Model
600172
Company Name
Liebel-Flarsheim Company LLC
Labeler DUNS
080186051
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
7
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
6b9543e8-6799-49fb-b75a-ee2d85d01741
Distribution End Date
2021-12-14

Device Description

Angio / CT Syringe with Handi-Fil Straw; fits injectors: OptiStat and Angiomat 6000

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DXT Injector And Syringe, Angiographic

GMDN Terms

Code Name
15286 Angiographic syringe

Identifiers

Type ID
Primary 10746190002017
Package 20746190002014

Premarket Submissions

Submission Number Supplement Number
K860204 000

Device Sizes

Type Value Unit Text
Total Volume 130 Milliliter