FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 60801902123093 · Model: IPN036969 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
60801902123093
Version / Model
IPN036969
Catalog Number
AK-11802-F
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-04
Public Version
6
Public Version Date
2022-03-14
Public Version Status
Update
Public Device Record Key
c9b2d4d8-a676-4eda-a1db-3896f2cd63b2

Device Description

Pediatric Two-Lumen Hemodialysis Catheterization

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MPB CATHETER, HEMODIALYSIS, NON-IMPLANTED

GMDN Terms

Code Name
46979 Double-lumen haemodialysis catheter, nonimplantable

Identifiers

Type ID
Previous 30801902123092
Package 50801902123096
Primary 60801902123093

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 8 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
20 – 25 Degrees Celsius