FDA UDI
In Commercial Distribution
🇺🇸 United States
Boomerang
DI: 00860013182311
·
Model: BMGPVT125
·
Aveera Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Boomerang
- Primary DI
- 00860013182311
- Version / Model
- BMGPVT125
- Company Name
- Aveera Medical Inc.
- Labeler DUNS
- 119410497
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2025-07-14
- Public Version
- 1
- Public Version Date
- 2025-07-22
- Public Version Status
- New
- Public Device Record Key
- 95ddef0d-18a9-4e90-99c9-288d6f251ca0
Device Description
The Boomerang Push Valvulotome is an over-the-wire (OTW) catheter designed to disrupt venous valves in the lower limb. The catheter is positioned percutaneously under fluoroscopic guidance such that the distal tip is advanced across the target venous valve. The catheter has a self-centering basket with shielded cutting blades. As the catheter is advanced, the basket cutting elements disrupt the venous valves, facilitating retrograde vein flow.
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
- Yes
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| MGZ | Valvulotome | Cardiovascular | 870.4885 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 62527 | Valvulotome, percutaneous | A sterile, flexible tube with an exposable blade assembly at its distal end designed to incise/excise peripheral venous valves to allow retrograde flow of blood. It is introduced percutaneously over an in-situ guidewire into a vein before being advanced distally to the valves, where the cutting implement is exposed using controls at the proximal end. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00860013182311 | GS1 |
Customer Contacts
- Phone
- 4405671793
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K250105 | 000 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Catheter Working Length | 125 | Centimeter | |
| Catheter Gauge | 4 | French | |
| Guidewire Diameter | 0.018 | Inch |