Triple-Loop Snare Retrieval Kit

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name: Triple-Loop Snare Retrieval Kit FDA UDI
Generic Name: Vena cava filter extraction/repositioning kit FDA UDI
Device Name: Triple-Loop Snare Retrieval Kit FDA UDI
Model / Reference: 380911330 FDA UDI
Description: Triple-Loop Snare Retrieval Kit FDA UDI

Identifiers

Catalog Number: 380911330 FDA UDI
Primary DI / UDI-DI: 00886333224616 FDA UDI
510(k) Number: K191758 FDA UDI
FDA Product Code: MMX FDA UDI
GMDN Term: Vena cava filter extraction/repositioning kit 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

Yes

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

Yes

FDA UDI

Category: Vena cava filter extraction/repositioning kit

Triple-Loop Snare Retrieval Kit by Argon Medical Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vena cava filter extraction/repositioning kit.

RECOVERY CONE® — Bard Peripheral Vascular · Class II
Bard Snare US — HERAEUS MEDICAL COMPONENTS LLC · Class II
CavaClear laser sheath — Philips Image Guided Therapy Corporation · Class II
CavaClear laser sheath — Philips Image Guided Therapy Corporation · Class II
RECOVERY CONE® — Bard Peripheral Vascular · Class II
Single-Loop Snare Retrieval Kit — Argon Medical Devices, Inc. · Class II

Cleared under the same submission

K191758 also covers:

Single-Loop Snare Retrieval Kit — Argon Medical Devices, Inc.

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: Argon Medical Devices, Inc.

Sources (1)

FDA UDI 77fd2414-5312-41ed-8b1d-5e18e9f5a577 37 fields · synced Jun 9, 2026