FDA UDI In Commercial Distribution 🇺🇸 United States

Q-Rejuvalight Pro Facewear

DI: 08719327598719 · Model: P19-0023 · Light Tree Ventures Europe B.V.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Q-Rejuvalight Pro Facewear
Primary DI
08719327598719
Version / Model
P19-0023
Company Name
Light Tree Ventures Europe B.V.
Labeler DUNS
493246808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-05
Public Version
1
Public Version Date
2024-03-13
Public Version Status
New
Public Device Record Key
fc5fe225-7df4-4504-a6a6-a2be3e742a12

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OHS Light Based Over The Counter Wrinkle Reduction
OLP Over-The-Counter Powered Light Based Laser For Acne

GMDN Terms

Code Name
47704 Cosmetic red-light phototherapy system, home-use
62116 Red/blue light phototherapy unit

Identifiers

Type ID
Primary 08719327598719

Premarket Submissions

Submission Number Supplement Number
K230042 000