FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 20801902162001 · Model: IPN915328 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
ARROW
Primary DI
20801902162001
Version / Model
IPN915328
Catalog Number
IAK-S8IT
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-15
Public Version
4
Public Version Date
2024-03-20
Public Version Status
Update
Public Device Record Key
59160c3f-4c88-4cf4-9277-9149b015b7cc

Device Description

Percutaneous Insertion Tray

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
DSP System, balloon, intra-aortic and control

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Package 10801902162004
Primary 20801902162001

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K981660 000