FDA UDI In Commercial Distribution 🇺🇸 United States

L3 LIGHT GUIDE

DI: 04719873120567 · Model: LD1009-171 · BONART CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
L3 LIGHT GUIDE
Primary DI
04719873120567
Version / Model
LD1009-171
Company Name
BONART CO., LTD.
Labeler DUNS
657263687
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
4
Public Version Date
2018-07-31
Public Version Status
Update
Public Device Record Key
2774f446-19da-4a5d-b04b-40d6fef5f8ea

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EBZ Activator, Ultraviolet, For Polymerization

GMDN Terms

Code Name
35761 Dental laboratory curing unit

Identifiers

Type ID
Primary 04719873120567

Premarket Submissions

Submission Number Supplement Number
K062289 000