FDA UDI In Commercial Distribution 🇺🇸 United States

Intensity Pulsed Light Therapy System

DI: 06970453270265 · Model: VE2000 Pro · Beijing ADSS Development Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intensity Pulsed Light Therapy System
Primary DI
06970453270265
Version / Model
VE2000 Pro
Company Name
Beijing ADSS Development Co., Ltd.
Labeler DUNS
529128739
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-30
Public Version
1
Public Version Date
2025-11-07
Public Version Status
New
Public Device Record Key
a7d10254-e055-4cb6-bb80-0593d4db28f1

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
58935 Intense pulsed light skin surface treatment system

Identifiers

Type ID
Primary 06970453270265

Premarket Submissions

Submission Number Supplement Number
K233307 000