FDA UDI In Commercial Distribution 🇺🇸 United States

LF

DI: 10746190004752 · Model: 802622 · Liebel-Flarsheim Company LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LF
Primary DI
10746190004752
Version / Model
802622
Company Name
Liebel-Flarsheim Company LLC
Labeler DUNS
080186051
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
5
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
96a1e508-9452-46a5-bf4a-2e9f59c09e43

Device Description

Hand Button Start Switch (Accessory)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
IZQ Injector, Contrast Medium, Automatic

GMDN Terms

Code Name
58000 CT contrast medium injection system, line-powered, stationary

Identifiers

Type ID
Primary 10746190004752

Premarket Submissions

Submission Number Supplement Number
K063503 000

Device Sizes

Type Value Unit Text
Length 20 Feet
Length 6 Meter