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VNS Therapy® Model 302 Lead

FDA UDI

Class III (US FDA UDI)

by LivaNova USA, Inc.

Identity

Trade Name
VNS Therapy® Model 302 Lead FDA UDI
Generic Name
Vagus nerve electrical stimulation system lead FDA UDI
Device Name
Implantable Bipolar Lead FDA UDI
Model / Reference
302-20 FDA UDI
Description
Implantable Bipolar Lead FDA UDI

Identifiers

Primary DI / UDI-DI
05425025750092 FDA UDI
PMA Number
P970003 FDA UDI
FDA Product Code
MUZ FDA UDI
LYJ FDA UDI
GMDN Term
Vagus nerve electrical stimulation system lead 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.0 Millimeter FDA UDI

Category: Vagus nerve electrical stimulation system lead

VNS Therapy® Model 302 Lead by LivaNova USA, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vagus nerve electrical stimulation system lead.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LivaNova USA, Inc.

Sources (1)

  • FDA UDI 3b64a7bb-9683-47dd-a632-39ddf32ecc67 37 fields · synced Jun 8, 2026