FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902001013 · Model: IPN035767 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902001013
Version / Model
IPN035767
Catalog Number
IV-01100
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-29
Public Version
26
Public Version Date
2024-01-10
Public Version Status
Update
Public Device Record Key
febcf2e9-9e0d-478d-88f5-8e76a7db4a83

Device Description

Twin-Cath(R) 20/22 Two-Lumen Peripheral 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
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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days

GMDN Terms

Code Name
36257 Peripherally-inserted central venous catheter

Identifiers

Type ID
Package 50801902001011
Package 40801902001014
Primary 10801902001013

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K862153 000