← Back to catalogue

Battery Charger

FDA UDI

Class II (US FDA UDI)

by Stimwave Technologies Incorporated

Identity

Trade Name
Battery Charger FDA UDI
Generic Name
Noninvasive device battery charger FDA UDI
Device Name
Freedom Spinal Cord Stimulator System/StimQ Peripheral Nerve Stimulator System Battery Charger FDA UDI
Model / Reference
MD0567-R1 FDA UDI
Description
Freedom Spinal Cord Stimulator System/StimQ Peripheral Nerve Stimulator System Battery Charger FDA UDI

Identifiers

Primary DI / UDI-DI
00818225020891 FDA UDI
510(k) Number
K170141 FDA UDI
K171366 FDA UDI
FDA Product Code
GZF FDA UDI
GZB FDA UDI
GMDN Term
Noninvasive device battery charger FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5870 FDA UDI
882.5880 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Noninvasive device battery charger

Battery Charger by Stimwave Technologies Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive device battery charger.

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

Sources (1)

  • FDA UDI d54476ab-613a-412e-898e-f07487e77c02 34 fields · synced May 30, 2026