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VNS Therapy® Programming Wand Model 2000

FDA UDI

Class III (US FDA UDI)

by LivaNova USA, Inc.

Identity

Trade Name
VNS Therapy® Programming Wand Model 2000 FDA UDI
Generic Name
Vagus nerve electrical stimulation system programmer FDA UDI
Device Name
Programming Wand FDA UDI
Model / Reference
2000 FDA UDI
Description
Programming Wand FDA UDI

Identifiers

Primary DI / UDI-DI
05425025750177 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
MRI Safety
MR Unsafe FDA UDI

Category: Vagus nerve electrical stimulation system programmer

VNS Therapy® Programming Wand Model 2000 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

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 2d5d3e1b-2921-4d34-95f5-ab0269ec8364 36 fields · synced Jun 8, 2026