Headway

FDA UDI

Class II (US FDA UDI)

by Microvention Inc.

Identity

Trade Name: HEADWAY FDA UDI
Generic Name: Vascular microcatheter FDA UDI
Device Name: Headway Duo FDA UDI
Model / Reference: MC162167S-AL FDA UDI
Description: Headway Duo FDA UDI

Identifiers

Catalog Number: MC162167S FDA UDI
Primary DI / UDI-DI: 00842429117415 FDA UDI
FDA Product Code: DQO FDA UDI
GMDN Term: Vascular microcatheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1200 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

Yes

FDA UDI

Category: Vascular microcatheter

Headway by Microvention Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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PROWLER — Medos International Sàrl · Class II
Merit Maestro® — Merit Medical Systems, Inc. · Class II
Lantern Delivery Catheter — PENUMBRA, INC. · Class II
Direxion™ Fathom™-16 System — Boston Scientific · 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: Microvention Inc.

Sources (1)

FDA UDI 1924fe79-1d5a-4514-9852-4cb45c8c2d25 36 fields · synced May 30, 2026