FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902170634 · Model: IPN917347 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902170634
Version / Model
IPN917347
Catalog Number
9079-VC-005
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-19
Public Version
1
Public Version Date
2020-10-27
Public Version Status
New
Public Device Record Key
266a3624-3941-45e3-b3bd-72e4de58e1ea

Device Description

EZ-IO(R) 45mm Needle Set

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
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
FMI Needle, hypodermic, single lumen

GMDN Terms

Code Name
18009 Intraosseous infusion kit

Identifiers

Type ID
Package 20801902170631
Primary 10801902170634
Package 30801902170638

Customer Contacts