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emPOWER

FDA UDI

Class II (US FDA UDI)

by Bionx Medical Technologies, Inc.

Identity

Trade Name
emPOWER FDA UDI
Generic Name
Noninvasive device battery charger FDA UDI
Device Name
emPOWER Battery Charger FDA UDI
Model / Reference
em3 FDA UDI
Description
emPOWER Battery Charger FDA UDI

Identifiers

Primary DI / UDI-DI
B155EM30 FDA UDI
FDA Product Code
ISW FDA UDI
GMDN Term
Noninvasive device battery charger FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3500 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Noninvasive device battery charger

emPOWER by Bionx Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive device battery charger.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI abdf1a33-094c-443a-8e20-fb6f25d7e40b 33 fields · synced May 30, 2026