Identity
- Trade Name
- LimFlow Vector FDA UDI
- Generic Name
- Valvulotome, percutaneous FDA UDI
- Device Name
- The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves FDA UDI
- Model / Reference
- VT-US-23 FDA UDI
- Description
- The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850041730134 FDA UDI
- FDA Product Code
- MGZ FDA UDI
- GMDN Term
- Valvulotome, percutaneous FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4885 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Valvulotome, percutaneous
LimFlow Vector by Limflow Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Valvulotome, percutaneous.
- Boomerang — Aveera Medical, Inc. · Class II
- Boomerang — Aveera Medical, Inc. · Class II
- Eze-Sit Valvulotome — LeMaitre Vascular, Inc. · Class II
- LimFlow Vector — Limflow Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Limflow Inc.
Sources (1)
- FDA UDI 602dcf4b-048b-425d-84ad-fa86c88c6db9 33 fields · synced Jun 1, 2026