FDA UDI In Commercial Distribution 🇺🇸 United States

VenSure Balloon Dilation System

DI: 04260759931246 · Model: 1 · Fiagon GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VenSure Balloon Dilation System
Primary DI
04260759931246
Version / Model
1
Catalog Number
E 01 3526
Company Name
Fiagon GmbH
Labeler DUNS
312623008
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-10
Public Version
3
Public Version Date
2024-01-08
Public Version Status
Update
Public Device Record Key
f48de5d9-76f2-4c51-925f-94e855b144f1

Device Description

Balloon Dilation system as set including Balloon dilation device with bending tool and Inflation device with tubes,

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LRC Instrument, Ent Manual Surgical
PNZ Eustachian Tube Balloon Dilation Device

GMDN Terms

Code Name
48140 Nasal/paranasal balloon catheter

Identifiers

Type ID
Package 04260759932243
Primary 04260759931246
Package 14260759931243