FDA UDI In Commercial Distribution 🇺🇸 United States

Apilux

DI: 00686209171125 · Model: SmartPro II · Dectro International
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Apilux
Primary DI
00686209171125
Version / Model
SmartPro II
Catalog Number
01-7112
Company Name
Dectro International
Labeler DUNS
246237945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-22
Public Version
5
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
6e2ac422-8a88-4ade-b65a-fb1e6981bee9

Device Description

Intense Pulsed Light (IPL) for Treatment of Acne, Vascular Lesions, Pigemented Lesions, Light Hair Removal, Dark HairRemoval

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 00686209171125

Premarket Submissions

Submission Number Supplement Number
K093168 000