← Back to catalogue

Senza

FDA UDI

Class III (US FDA UDI)

by Nevro Corporation

Identity

Trade Name
Senza FDA UDI
Generic Name
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator FDA UDI
Device Name
Bluetooth Trial stimulator kit FDA UDI
Model / Reference
EXTS3000 FDA UDI
Description
Bluetooth Trial stimulator kit FDA UDI

Identifiers

Catalog Number
EXTS3000 FDA UDI
Primary DI / UDI-DI
00813426020664 FDA UDI
PMA Number
P130022 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator 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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator

Senza by Nevro Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator.

Cleared under the same submission

P130022 also covers:

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
Nevro Corporation

Sources (1)

  • FDA UDI f5d1e4b4-fc3c-4257-9fcf-51f6c0186e60 36 fields · synced Jun 8, 2026