FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 50801902012130 · Model: IPN033217 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
50801902012130
Version / Model
IPN033217
Catalog Number
MS-02041-T
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-17
Public Version
3
Public Version Date
2019-11-13
Public Version Status
Update
Public Device Record Key
fe7c660f-845b-46db-b676-fb95dc8e556c

Device Description

Peripherally Inserted Midline Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
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
LJS Catheter, intravascular, therapeutic, long-term greater than 30 days

GMDN Terms

Code Name
40601 Peripheral vascular catheter

Identifiers

Type ID
Package 40801902012133
Primary 50801902012130

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K963257 000