← Back to catalogue

Bon Charge

FDA UDI

Class II (US FDA UDI)

by Blublox Pty Ltd

Identity

Trade Name
BON CHARGE FDA UDI
Generic Name
Cosmetic red-light phototherapy system, home-use FDA UDI
Model / Reference
Mini Red Light Therapy Device FDA UDI

Identifiers

Primary DI / UDI-DI
09361725000074 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Cosmetic red-light phototherapy system, home-use 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cosmetic red-light phototherapy system, home-use

Bon Charge by Blublox Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic red-light phototherapy system, home-use.

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
Blublox Pty Ltd

Sources (1)

  • FDA UDI 287905af-3046-49bd-9028-f6ad302f5294 32 fields · synced May 30, 2026