FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10816000013738 · Model: IPN033741 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10816000013738
Version / Model
IPN033741
Catalog Number
9055
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-12
Public Version
4
Public Version Date
2022-11-23
Public Version Status
Update
Public Device Record Key
fe7995b5-5020-4738-abaa-4aaf577c9079

Device Description

Manual 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
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
KNW INSTRUMENT, BIOPSY

GMDN Terms

Code Name
18009 Intraosseous infusion kit

Identifiers

Type ID
Package 30816000013732
Package 20816000013735
Primary 10816000013738

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K091140 000