Option Elite Retrievable Vena Cava Filter

FDA UDI

Class II (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name: Option Elite Retrievable Vena Cava Filter FDA UDI
Generic Name: Vena cava filter, temporary/permanent FDA UDI
Device Name: Option Elite Retrievable Vena Cava Filter Suitable for Antecubital or Popliteal Delivery FDA UDI
Model / Reference: 352506100E FDA UDI
Description: Option Elite Retrievable Vena Cava Filter Suitable for Antecubital or Popliteal Delivery FDA UDI

Identifiers

Catalog Number: 352506100E FDA UDI
Primary DI / UDI-DI: 00886333222346 FDA UDI
FDA Product Code: DTK FDA UDI
GMDN Term: Vena cava filter, temporary/permanent FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.3375 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Vena cava filter, temporary/permanent

Option Elite Retrievable Vena Cava Filter 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, temporary/permanent.

Cook Celect — William Cook Europe ApS · Class II
Cook Celect — William Cook Europe ApS · Class II
Simon Nitinol Filter™ — Bard Peripheral Vascular · Class II
Angel Catheter — Bio2 Medical, Inc. · Class II
Gunther Tulip — COOK INCORPORATED · Class II
Gunther Tulip — COOK INCORPORATED · Class II
Gunther Tulip — COOK INCORPORATED · Class II
ALN Optional Vena Cava Filter - Brachial Approach — A.L.N. · 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: Argon Medical Devices, Inc.

Sources (1)

FDA UDI 558563d8-b1b8-46cd-971f-99dda552ca18 37 fields · synced Jun 9, 2026