Apilux 01-9220

GUDID 00686209192205

Intense Pulsed Light unit (IPL) 220Vac

Dectro International

Multi-modality skin surface treatment system
Primary Device ID00686209192205
NIH Device Record Key6703d900-9ec0-4f88-b9ba-013c2ec42927
Commercial Distribution StatusIn Commercial Distribution
Brand NameApilux
Version Model NumberAPL3G 220V
Catalog Number01-9220
Company DUNS246237945
Company NameDectro International
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100686209192205 [Primary]

FDA Product Code

ONFPowered Light Based Non-Laser Surgical Instrument With Thermal Effect

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-11
Device Publish Date2021-05-03

On-Brand Devices [Apilux]

06862090171121Intense Pulsed Light (IPL) for Treatment of Acne, Vascular Lesions, Pigemented Lesions, Light Ha
06862090171022Intense Pulsed Ligh (ILP) for Light Hair Removal abd Dark Hair Removal
00686209171125Intense Pulsed Light (IPL) for Treatment of Acne, Vascular Lesions, Pigemented Lesions, Light Ha
00686209171026Intense Pulsed Ligh (ILP) for Light Hair Removal abd Dark Hair Removal
00686209192205Intense Pulsed Light unit (IPL) 220Vac
00686209191109Intense Pulsed Light unit (IPL) 120Vac

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.