FDA UDI In Commercial Distribution 🇺🇸 United States

ARROW

DI: 10801902206432 · Model: IPN922644 · TELEFLEX INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ARROW
Primary DI
10801902206432
Version / Model
IPN922644
Catalog Number
AI-07127
Company Name
TELEFLEX INCORPORATED
Labeler DUNS
002348191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-10-20
Public Version
2
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
bdec63a5-0566-43fc-9566-045b1ccf1220

Device Description

CATH PKGD: WEDGE 7 FR 110 CM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
DYG CATHETER, FLOW DIRECTED

GMDN Terms

Code Name
35889 Pulmonary artery balloon catheter, non-electrical

Identifiers

Type ID
Package 20801902206439
Primary 10801902206432

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K892530 000

Device Sizes

Type Value Unit Text
Length 110 Centimeter
Catheter Gauge 7 French

Storage Conditions

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