← Back to catalogue

Paired VNS

FDA UDI

Class III (US FDA UDI)

by Microtransponder

Identity

Trade Name
Paired VNS FDA UDI
Generic Name
Vagus nerve electrical stimulation system programmer FDA UDI
Device Name
Wireless Transmitter FDA UDI
Model / Reference
2000 FDA UDI
Description
Wireless Transmitter FDA UDI

Identifiers

Primary DI / UDI-DI
10810041430042 FDA UDI
PMA Number
P210007 FDA UDI
FDA Product Code
QPY 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

Paired VNS by Microtransponder — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Microtransponder

Sources (1)

  • FDA UDI 5404a351-0b08-4580-bdfe-001559e68dc1 34 fields · synced May 30, 2026