FDA UDI In Commercial Distribution 🇺🇸 United States

ATL

DI: 06970507240022 · Model: Angelite-DDC · Advanced Technology Laser Co.,Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATL
Primary DI
06970507240022
Version / Model
Angelite-DDC
Company Name
Advanced Technology Laser Co.,Ltd.
Labeler DUNS
547070719
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-20
Public Version
4
Public Version Date
2021-10-19
Public Version Status
Update
Public Device Record Key
35e79f9d-9914-4a85-810c-3fab48b669f0

Device Characteristics

Single Use
Yes
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
MR Unsafe
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
Yes

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 06970507240022

Premarket Submissions

Submission Number Supplement Number
K083915 000