FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 30801902167300 · Model: IPN916982 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
30801902167300
Version / Model
IPN916982
Catalog Number
ASK-04000-HMC
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-30
Public Version
1
Public Version Date
2022-04-07
Public Version Status
New
Public Device Record Key
87edbf16-51ac-4c14-9b60-e2a1f30980fb

Device Description

Prep Tray

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
DQY Catheter, percutaneous

GMDN Terms

Code Name
10729 Centrally-inserted central venous catheter

Identifiers

Type ID
Package 40801902167307
Primary 30801902167300
Previous 10801902167306

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K862056 000