Nevro®

FDA UDI

Class III (US FDA UDI)

by Nevro Corporation

Identity

Trade Name: Nevro® FDA UDI
Generic Name: Medical device adhesive FDA UDI
Device Name: Medical Adhesive Kit FDA UDI
Model / Reference: ACCK9100 FDA UDI
Description: Medical Adhesive Kit FDA UDI

Identifiers

Catalog Number: ACCK9100 FDA UDI
Primary DI / UDI-DI: 00813426020343 FDA UDI
PMA Number: P130022 FDA UDI
FDA Product Code: LGW FDA UDI
GMDN Term: Medical device adhesive FDA UDI

Classification

Device Class: Class III FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device adhesive

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

Similar devices

Also classified as Medical device adhesive.

Argyle — Mozarc Medical US LLC · Class II
Kangaroo — Cardinalhealth · Class II
Precision ™ — Boston Scientific Neuromodulation · Class III
Alligator — Micro Therapeutics, Inc. · Class II
Alligator — Micro Therapeutics, Inc. · Class II
Alligator — Micro Therapeutics, Inc. · Class II
Devon — Cardinalhealth · Class I
Alligator — Micro Therapeutics, Inc. · Class II

Cleared under the same submission

P130022 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class III	Pending data

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

Manufacturer

Manufacturer: Nevro Corporation

Sources (1)

FDA UDI e3d600f1-d8e0-47c3-81f4-ef84ce4e5422 36 fields · synced May 30, 2026