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VNS Therapy® Model 250 v11.0 Programming Software

FDA UDI

Class III (US FDA UDI)

by LivaNova USA, Inc.

Identity

Trade Name
VNS Therapy® Model 250 v11.0 Programming Software FDA UDI
Generic Name
Vagus nerve electrical stimulation system programmer FDA UDI
Device Name
Programming Software FDA UDI
Model / Reference
250 v11.0 FDA UDI
Description
Programming Software FDA UDI

Identifiers

Primary DI / UDI-DI
05425025750368 FDA UDI
PMA Number
P970003 FDA UDI
FDA Product Code
MUZ FDA UDI
LYJ FDA UDI
GMDN Term
Vagus nerve electrical stimulation system programmer FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vagus nerve electrical stimulation system programmer

VNS Therapy® Model 250 v11.0 Programming Software 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 programmer.

Cleared under the same submission

P970003 also covers:

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 593bfcd4-dec1-4cb1-991b-86204ef664ef 36 fields · synced Jun 8, 2026