FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902167733 · Model: IPN915319 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902167733
Version / Model
IPN915319
Catalog Number
IAB-05840-LWS
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-06
Public Version
4
Public Version Date
2023-11-06
Public Version Status
Update
Public Device Record Key
1a8d3da3-0788-4369-8602-2ac985eef607

Device Description

RediGuard(R) IAB

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
Yes
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
34919 Intra-aortic balloon catheter

Identifiers

Type ID
Primary 10801902167733

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 8 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at normal room temperature away from direct exposure to light. Prolonged exposure to fluorescent light, sunlight or heat will damage the balloon