Oxylight

FDA UDI

Class II (US FDA UDI)

by RAJA Medical

Identity

Trade Name: OXYLIGHT FDA UDI
Generic Name: Multi-modality skin surface treatment system FDA UDI
Device Name: The JUVESAPROSKIN System is a multi-modality skin surface treatment system that uses multiple therapeutic modalities delivered through different attachments or handles connected to a main body. The system includes various handles that deliver a variety of therapeutic modalities including microdermabrasion, LED light and Oxygen spray. FDA UDI
Model / Reference: JUVESA PROSKIN FDA UDI
Description: The JUVESAPROSKIN System is a multi-modality skin surface treatment system that uses multiple therapeutic modalities delivered through different attachments or handles connected to a main body. The system includes various handles that deliver a variety of therapeutic modalities including microdermabrasion, LED light and Oxygen spray. FDA UDI

Identifiers

Catalog Number: JUVESA PROSKIN FDA UDI
Primary DI / UDI-DI: G050JUVESAPROSKIN0 FDA UDI
FDA Product Code: GEX FDA UDI
GFE FDA UDI
GMDN Term: Multi-modality skin surface treatment system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4810 FDA UDI
878.4820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Multi-modality skin surface treatment system

Oxylight by RAJA Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: RAJA Medical

Sources (1)

FDA UDI a9ebdca8-1aeb-482b-94ba-49fe12b3e107 34 fields · synced May 30, 2026