Omnia

FDA UDI

Class III (US FDA UDI)

by Nevro Corporation

Identity

Trade Name: Omnia FDA UDI
Generic Name: Personal device holder, reusable FDA UDI
Device Name: Charger 2500 Power Supply Kit FDA UDI
Model / Reference: CHPS2500 FDA UDI
Description: Charger 2500 Power Supply Kit FDA UDI

Identifiers

Catalog Number: CHPS2500 FDA UDI
Primary DI / UDI-DI: 00813426020626 FDA UDI
PMA Number: P130022 FDA UDI
FDA Product Code: LGW FDA UDI
GMDN Term: Personal device holder, reusable FDA UDI

Classification

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

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Personal device holder, reusable

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

Similar devices

Also classified as Personal device holder, reusable.

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Personal Device Holder — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class I
Leg Bag Holder Small — FLEXICARE MEDICAL LIMITED · Class I
CADD — ICU MEDICAL, INC. · Class II
Kangaroo — Cardinalhealth · Class I
Conveen — Coloplast A/S · Class I
Axonics — AXONICS MODULATION TECHNOLOGIES, INC. · Class III

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

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Manufacturer

Manufacturer: Nevro Corporation

Sources (1)

FDA UDI 3dbda3cc-0611-4d5a-967a-0cb6a77863db 36 fields · synced Jun 1, 2026