Ml 830®

FDA UDI

Class II (US FDA UDI)

by Microlight Corporation Of America

Identity

Trade Name: ML 830® FDA UDI
Generic Name: Noninvasive device battery charger FDA UDI
Device Name: Charging Station FDA UDI
Model / Reference: ML-830-01-001 FDA UDI
Description: Charging Station FDA UDI

Identifiers

Catalog Number: ML-830-01-001 FDA UDI
Primary DI / UDI-DI: 00859626006015 FDA UDI
FDA Product Code: NHN FDA UDI
GMDN Term: Noninvasive device battery charger FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5500 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

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Noninvasive device battery charger

Ml 830® by Microlight Corporation Of America — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Noninvasive device battery charger.

STARKEY HEARING TECHNOLOGIES — Starkey Laboratories Inc. · Class II
GN Hearing — Gn Hearing A/S · Class II
CONNEXX — WS Audiology USA, Inc. · Class II
Unitron Brand — Sonova AG · Class II
Beltone — Gn Hearing A/S · Class II
GN Hearing — Gn Hearing A/S · Class II
Docking Station — Medela LLC · Class II
GN Hearing — Gn Hearing A/S · Class II

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 II	Pending data

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

Manufacturer

Manufacturer: Microlight Corporation Of America

Sources (1)

FDA UDI 94a62e61-2349-4a3a-9a81-d34dd55702aa 35 fields · synced May 30, 2026