FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 70801902113381 · Model: IPN037285 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
70801902113381
Version / Model
IPN037285
Catalog Number
ASK-05052-DMI
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
3
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
7a33046b-95e2-463b-b37d-8b22671a6878

Device Description

Pressure Injectable Two-Lumen Peripherally Inserted Central Catheter Kit

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
Yes
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
LJT PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

GMDN Terms

Code Name
36257 Peripherally-inserted central venous catheter

Identifiers

Type ID
Package 60801902113384
Primary 70801902113381

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K003006 000