FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902198805 · Model: IPN920866 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902198805
Version / Model
IPN920866
Catalog Number
PR-35563-HPSM
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-16
Public Version
2
Public Version Date
2024-01-10
Public Version Status
Update
Public Device Record Key
77531208-22c1-4d93-bc9a-2145adc0cd42

Device Description

Pressure Injectable Three-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
Yes
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 20801902198802
Primary 10801902198805

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K003006 000