FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 50801902123102 · Model: IPN036965 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
ARROW
Primary DI
50801902123102
Version / Model
IPN036965
Catalog Number
AK-12122-F
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-23
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
d1b1c50d-b921-4a84-8fbd-4dde03347e99

Device Description

Two-Lumen Hemodialysis Catheterization Kit 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
Yes
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
No
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 60801902123109
Primary 50801902123102

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K895417 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius