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Nevro®

FDA UDI

Class III (US FDA UDI)

by Nevro Corporation

Identity

Trade Name
Nevro® FDA UDI
Generic Name
Central nervous system electrical stimulation system lead stylet FDA UDI
Device Name
Style Kit, 30cm Length FDA UDI
Model / Reference
ACCK8012-30 FDA UDI
Description
Style Kit, 30cm Length FDA UDI

Identifiers

Catalog Number
ACCK8012-30 FDA UDI
Primary DI / UDI-DI
00813426020299 FDA UDI
PMA Number
P130022 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Central nervous system electrical stimulation system lead stylet 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Central nervous system electrical stimulation system lead stylet

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

Similar devices

Also classified as Central nervous system electrical stimulation system lead stylet.

Cleared under the same submission

P130022 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nevro Corporation

Sources (1)

  • FDA UDI 646e0ef4-7c70-41e3-9e04-e457e2e8b472 36 fields · synced Jun 1, 2026