FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902095388 · Model: IPN033362 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902095388
Version / Model
IPN033362
Catalog Number
PR-05052-HP
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
10
Public Version Date
2023-08-08
Public Version Status
Update
Public Device Record Key
78d75410-711d-4fb4-b75a-daf6939ecf30

Device Description

Pressure Injectable Two-Lumen PICC with 80 cm Wire

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
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
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
36257 Peripherally-inserted central venous catheter

Identifiers

Type ID
Package 20801902095385
Primary 10801902095388

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K042126 000