FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902219401 · Model: EDC-00820 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902219401
Version / Model
EDC-00820
Catalog Number
EDC-00820
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-24
Public Version
1
Public Version Date
2026-04-01
Public Version Status
New
Public Device Record Key
589895d4-98be-43fc-ab39-cf336ce885d5

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
Yes
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Safe
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
64574 Peripheral intravenous cannula

Identifiers

Type ID
Package 30801902219405
Package 20801902219408
Primary 10801902219401

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242281 000