LimFlow V-Ceiver

FDA UDI

Class II (US FDA UDI)

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-21 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: 00850041730004 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Intravascular extraction catheter-snare

LimFlow V-Ceiver by Limflow Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular extraction catheter-snare.

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NCircle — COOK INCORPORATED · Class I
EN Snare® — Merit Medical Systems, Inc. · Class II
ONO Retrieval Device — Onocor LLC · Class II
Amplatz Goose Neck™ — MEDTRONIC, INC. · Class II
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 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

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Manufacturer

Manufacturer: Limflow Inc.

Sources (1)

FDA UDI 7674acbf-ee7c-4a46-925f-3610442c3baf 34 fields · synced May 30, 2026