FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902190236 · Model: IPN919711 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902190236
Version / Model
IPN919711
Catalog Number
CS-15122-E
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-29
Public Version
2
Public Version Date
2023-07-19
Public Version Status
Update
Public Device Record Key
d0956318-1513-4d80-a4e0-aa9d08dec1ef

Device Description

Two-Lumen Hemodialysis Catheterization Set with Blue FlexTip(R) Catheter for High Volume Infusions

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
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
LFJ Catheter, subclavian

GMDN Terms

Code Name
46979 Double-lumen haemodialysis catheter, nonimplantable

Identifiers

Type ID
Package 20801902190233
Primary 10801902190236

Customer Contacts