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Neuroform Ez 3

FDA UDI

Class Unclassified (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
NEUROFORM EZ 3 FDA UDI
Generic Name
Bare-metal intracranial vascular stent FDA UDI
Device Name
Stent System FDA UDI
Model / Reference
M003N3EZ25200 FDA UDI
Description
Stent System FDA UDI

Identifiers

Catalog Number
M003N3EZ25200 FDA UDI
Primary DI / UDI-DI
04546540697745 FDA UDI
PMA Number
H020002 FDA UDI
FDA Product Code
NJE FDA UDI
GMDN Term
Bare-metal intracranial vascular stent FDA UDI

Classification

Device Class
Unclassified 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 20.0 Millimeter FDA UDI
Outer Diameter — 2.5 Millimeter FDA UDI

Category: Bare-metal intracranial vascular stent

Neuroform Ez 3 by Stryker Corp. — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal intracranial vascular stent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI f2d9bf94-a85f-43ae-8e2f-84163d53d390 38 fields · synced May 30, 2026