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LimFlow V-Ceiver
FDA UDIFDA 510(k)Class II (US FDA UDI)
510(k) K222083
by Limflow Inc.
Identity
- Trade Name
- LimFlow V-Ceiver FDA UDI
- Generic Name
- Intravascular extraction catheter-snare FDA UDI
- Device Name
- The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve guidewires specified in the IFU. FDA UDI
- Model / Reference
- VC-US-23 FDA UDI
- Description
- The LimFlow V-Ceiver is intended for use in the cardiovascular system to manipulate and retrieve guidewires specified in the IFU. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850041730141 FDA UDI
- FDA Product Code
- MMX FDA UDI
- GMDN Term
- Intravascular extraction catheter-snare FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5150 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: Intravascular extraction catheter-snare
LimFlow V-Ceiver by Limflow Inc. — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Similar devices
Also classified as Intravascular extraction catheter-snare.
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- Halo™ Single-Loop Microsnare Kit — Argon Medical Devices, Inc. · Class II
- Halo™ Single-Loop Microsnare Kit — Argon Medical Devices, Inc. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K242776 | Class II | Active |
| FDA 510(k) | United States | FDA_510K | K222083 | Class II | Active |
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Manufacturer
- Manufacturer
- Limflow Inc.
- FDA Applicant
- LimFlow, Inc.
Sources (2)
- FDA UDI 0bb5381f-9970-4f96-8684-18ebf1e415a9 58 fields · synced Jun 18, 2026
- FDA 510(k) K242776 1 fields · synced May 29, 2026