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WEB Aneurysm Embolization System

FDA UDI

Class III (US FDA UDI)

by Microvention Inc.

Identity

Trade Name
WEB Aneurysm Embolization System FDA UDI
Generic Name
Neurovascular embolization coil FDA UDI
Device Name
WEB 27 SL 10x6 FDA UDI
Model / Reference
W2-10-6-MVI-3 FDA UDI
Description
WEB 27 SL 10x6 FDA UDI

Identifiers

Catalog Number
W2-10-6 FDA UDI
Primary DI / UDI-DI
00842429107263 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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Neurovascular embolization coil

WEB Aneurysm Embolization System by Microvention Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurovascular embolization coil.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microvention Inc.

Sources (1)

  • FDA UDI da512a09-1e39-43af-a18e-e9f255a7fdd6 37 fields · synced May 30, 2026