FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902219517 · Model: EDC-00822-HC · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902219517
Version / Model
EDC-00822-HC
Catalog Number
EDC-00822-HC
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
20899d83-ab11-47be-87a7-a200f7bfd75a

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
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 20801902219514
Primary 10801902219517

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242281 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Avoid freezing and excessive heat above 40C (104F)
Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius