← Back to catalogue

Senza

FDA UDI

Class III (US FDA UDI)

by Nevro Corporation

Identity

Trade Name
Senza FDA UDI
Generic Name
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable FDA UDI
Device Name
IPG Model IPG3000 Kit, NIPG3000 FDA UDI
Model / Reference
NIPG3000 FDA UDI
Description
IPG Model IPG3000 Kit, NIPG3000 FDA UDI

Identifiers

Catalog Number
NIPG3000 FDA UDI
Primary DI / UDI-DI
00813426020718 FDA UDI
PMA Number
P130022 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable

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

Similar devices

Also classified as Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, implantable.

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
Nevro Corporation

Sources (1)

  • FDA UDI f417ce9f-5817-4688-b496-446369dcbd82 35 fields · synced Jun 8, 2026