FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902210477 · Model: IPN925064 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902210477
Version / Model
IPN925064
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
2022-11-09
Public Version
2
Public Version Date
2023-08-29
Public Version Status
Update
Public Device Record Key
4f54e409-e554-4c9c-ad7f-fa4f8da48cb3

Device Description

Twin-Cath(R) 18/20 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
Yes
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 30801902210471
Package 20801902210474
Primary 10801902210477

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K862153 000