FDA UDI In Commercial Distribution 🇺🇸 United States

LF

DI: 10746190004233 · Model: 800099P · Liebel-Flarsheim Company LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
LF
Primary DI
10746190004233
Version / Model
800099P
Company Name
Liebel-Flarsheim Company LLC
Labeler DUNS
080186051
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-31
Public Version
1
Public Version Date
2022-01-10
Public Version Status
New
Public Device Record Key
1f5a79fe-d09e-436c-a3a3-7478000a78cb

Device Description

CT Syringe with Coiled Tubing and Filling Spike; fits injectors: OptiOne, OptiVantage and CT 9000 ADV

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
16545 Angiography kit

Identifiers

Type ID
Primary 10746190004233
Package 20746190004230
Package 30746190004237

Device Sizes

Type Value Unit Text
Pressure 2758 KiloPascal
Pressure 400 Pound per Square Inch
Total Volume 200 Milliliter