Optease

FDA UDI

Class II (US FDA UDI)

by Cordis Corp.

Identity

Trade Name: OPTEASE FDA UDI
Generic Name: Intravascular extraction catheter-snare FDA UDI
Device Name: 10FR OPTEASE RETRIEVAL CATH. FDA UDI
Model / Reference: 466C210F FDA UDI
Description: 10FR OPTEASE RETRIEVAL CATH. FDA UDI

Identifiers

Catalog Number: 466C210F FDA UDI
Primary DI / UDI-DI: 20705032009369 FDA UDI
FDA Product Code: DTK FDA UDI
GMDN Term: Intravascular extraction catheter-snare 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

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

MRI Safety

MR Conditional FDA UDI

Category: Intravascular extraction catheter-snare

Optease by Cordis Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 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: Cordis Corp.

Sources (1)

FDA UDI 237769d1-fd01-4d42-96db-b96b3aa4923d 35 fields · synced May 30, 2026