VenSure Balloon Dilation System
- Primary DI
- 04260759931246
- Brand
- VenSure Balloon Dilation System
- Company
- Fiagon GmbH
- Model
- 1
- Catalog number
- E 01 3526
- Device description
- Balloon Dilation system as set including Balloon dilation device with bending tool and Inflation device with tubes,
- Published
- 2022-11-10
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Product Codes#
Product Code Classifications#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04260759932243 | Package | GS1 | 5 | In Commercial Distribution |
| 14260759931243 | Package | GS1 | 5 | In Commercial Distribution |
| 04260759931246 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04260759932243 | 04260759932243 | 4260759932243 |
| 14260759931243 | 14260759931243 | |
| 04260759931246 | 04260759931246 | 4260759931246 |
GMDN Terms#
| Term | Definition |
|---|---|
| Nasal/paranasal balloon catheter, non-tracking | A flexible tube with an inflatable balloon at its distal tip designed to gently restructure nasal passages and dilate obstructed sinus ostia during a surgical procedure (sinuplasty), typically to treat sinusitis, and/or to gently restructure nasal passages to temporarily relieve nasal obstruction/congestion. The device typically consists of a single-lumen tube with a connector at the proximal end for attachment to an inflation device. This is a single-use device. |
Regulatory Flags#
- DUNS number
- 312623008
- Device count
- 1
- Kit
- true
- Lot or batch
- true
- Manufacturing date on label
- true
- Expiration date on label
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| EFIAE0135061 | VenSure Balloon Sinus Dilation System | 1 | E 01 3506 | 2021-06-11 |
| EFIAE0135161 | VenSure Nav Balloon Sinus Dilation System | 1 | 2021-06-11 | |
| 04260759931680 | VenSure 4D Balloon Dilation System | 1 | E 01 3566 | 2025-09-18 |
| 04260759931260 | VenSure Nav Balloon Dilation System | 1 | E 01 3546 | 2022-11-10 |
| 04260759931253 | VenSure Light Balloon Dilation System | 1 | E 01 3536 | 2022-10-14 |
| EFIAE0135921 | Vensure Inflation Device | 1 | E 01 3592 | 2022-01-21 |
| 04260759930003 | Integrated Headrest | E011970 | 2025-06-25 | |
| 04260759930133 | Navigation Unit Cube4D | E011106-HD/8 | E011106-HD/8 | 2025-01-16 |
| 04260759930157 | 4K Navigation Unit Cube4D | E011106-4K/8 | E011106-4K/8 | 2025-01-16 |
| 04260759930249 | Navigation Sensor | A011000 | A011000 | 2025-01-16 |
| 04260759930300 | FlexPointer | E012002 | E012002 | 2025-01-16 |
| 04260759930317 | FlexPointer 1.5 mm | E012004 | E012004 | 2025-01-16 |
| 04260759930324 | FlexTube 3mm | E012104 | E012104 | 2025-01-16 |
| 04260759930331 | FlexTube 4mm | E012106 | E012106 | 2025-01-16 |
| 04260759930348 | PointerTube Keat | E012107 | E012107 | 2025-01-16 |
| 04260759930355 | PointerTube Kennedy | E012108 | E012108 | 2025-01-16 |
| 04260759930447 | Localizer Adhesive Pad C-Type | E012202C | E012202C | 2025-01-16 |
| EFIAE012202C1 | Localizer Adhesive pad | C-Type | 2020-03-27 | |
| EFIAE0111060 | Fiagon Navigation Unit | CUBE4D | 2020-05-12 | |
| EFIAE0120021 | FlexPointer | 1 | 2016-08-05 |
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| 04059453133809 | Hermann Medizintechnik GmbH | Hermann Medizintechnik GmbH | LRC | 2026-07-16 |
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| 04250407721756 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
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| 04250407721831 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
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| 04250407722401 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
| 04250407722418 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
| 04250407722425 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
| 04250407722432 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
| 04250407722456 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
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| 04250407722500 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
| 04250407722517 | FENTEX | FENTEX medical GmbH | LRC | 2022-12-09 |
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