← Back to catalogue

GN Hearing

FDA UDI

Class II (US FDA UDI)

by Gn Hearing A/S

Identity

Trade Name
GN Hearing FDA UDI
Generic Name
Noninvasive device battery charger FDA UDI
Device Name
CHGR PREM,C-1 V3 GEN,CFF9 FDA UDI
Model / Reference
23325900 FDA UDI
Description
CHGR PREM,C-1 V3 GEN,CFF9 FDA UDI

Identifiers

Primary DI / UDI-DI
05708296367603 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Noninvasive device battery charger FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3305 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Noninvasive device battery charger

GN Hearing by Gn Hearing A/S — 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

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

Manufacturer

Manufacturer
Gn Hearing A/S

Sources (1)

  • FDA UDI fee61de9-261e-42be-8f4e-dc0b4e5df791 34 fields · synced May 30, 2026