FDA UDI Not in Commercial Distribution 🇺🇸 United States

Barrx

DI: 10884521189348 · Model: 32041-31 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Barrx
Primary DI
10884521189348
Version / Model
32041-31
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
17
Public Version Date
2025-06-24
Public Version Status
Update
Public Device Record Key
1ce5ee94-c40f-4fb5-b869-4f786542c422
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
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 10884521189348

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K083711 000

Device Sizes

Type Value Unit Text
Outer Diameter 31 Millimeter