FDA UDI In Commercial Distribution 🇺🇸 United States

LightLas 532

DI: 04712826770604 · Model: LC0013(3W) · LIGHTMED CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LightLas 532
Primary DI
04712826770604
Version / Model
LC0013(3W)
Company Name
LIGHTMED CORPORATION
Labeler DUNS
657731175
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
a31c5acc-83a5-485b-944e-d8fe18222a65

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HQF Laser, Ophthalmic

GMDN Terms

Code Name
36150 General/multiple surgical frequency-doubled solid-state laser system

Identifiers

Type ID
Primary 04712826770604

Premarket Submissions

Submission Number Supplement Number
K091534 000

Device Sizes

Type Value Unit Text
Weight 20 Kilogram