FDA UDI Not in Commercial Distribution 🇺🇸 United States

Barrx

DI: 10884521189331 · Model: 32041-28 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Barrx
Primary DI
10884521189331
Version / Model
32041-28
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
7
Public Version Date
2023-02-27
Public Version Status
Update
Public Device Record Key
74b24358-c32f-415b-a447-8e773435414f
Distribution End Date
2023-02-22

Device Description

360 RFA Balloon Catheter

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
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
45712 Gastrointestinal/biliary dilation balloon catheter

Identifiers

Type ID
Primary 10884521189331

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083711 000

Device Sizes

Type Value Unit Text
Outer Diameter 28 Millimeter