Web

FDA UDI

Class III (US FDA UDI)

by Microvention Inc.

Identity

Trade Name: WEB FDA UDI
Generic Name: Neurovascular embolization coil FDA UDI
Device Name: WEB 17 SL 5x4 FDA UDI
Model / Reference: W5-5-4-MVI-3 FDA UDI
Description: WEB 17 SL 5x4 FDA UDI

Identifiers

Catalog Number: W5-5-4 FDA UDI
Primary DI / UDI-DI: 00842429110867 FDA UDI
PMA Number: P170032 FDA UDI
FDA Product Code: OPR FDA UDI
GMDN Term: Neurovascular embolization coil FDA UDI

Classification

Device Class: Class III 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: Neurovascular embolization coil

Web by Microvention Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurovascular embolization coil.

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AxiumTM — Micro Therapeutics, Inc. · Class II
WEB Aneurysm Embolization System — SEQUENT MEDICAL, INC. · Class III
TARGET — Stryker Corp. · Class II
Axium™ Prime Detachable Coil System — Micro Therapeutics, Inc. · Class II
Axium™ Prime Detachable Coil System — Micro Therapeutics, Inc. · Class II
AxiumTM — Micro Therapeutics, Inc. · Class II

Cleared under the same submission

P170032 also covers:

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 III	Pending data

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Manufacturer

Manufacturer: Microvention Inc.

Sources (1)

FDA UDI bd84e704-7383-43d7-b627-c8ea6d1035ce 37 fields · synced Jun 1, 2026