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Nevro®

FDA UDI

Class III (US FDA UDI)

by Nevro Corporation

Identity

Trade Name
Nevro® FDA UDI
Generic Name
Implantable spinal cord electrical stimulation system programmer FDA UDI
Device Name
Programmer Kit FDA UDI
Model / Reference
CLPG2000 FDA UDI
Description
Programmer Kit FDA UDI

Identifiers

Catalog Number
CLPG2000 FDA UDI
Primary DI / UDI-DI
00813426020138 FDA UDI
PMA Number
P130022 FDA UDI
FDA Product Code
LGW FDA UDI
GMDN Term
Implantable spinal cord 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Implantable spinal cord electrical stimulation system programmer

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

Similar devices

Also classified as Implantable spinal cord 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
Nevro Corporation

Sources (1)

  • FDA UDI 50898d94-5a9f-4a11-a583-d069d1e5646f 36 fields · synced Jun 1, 2026