FDA UDI In Commercial Distribution 🇺🇸 United States

PeriOptix®

DI: D813AREPKITNA0 · Model: A-REPKIT-NA · DEN-MAT HOLDINGS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PeriOptix®
Primary DI
D813AREPKITNA0
Version / Model
A-REPKIT-NA
Catalog Number
A-REPKIT-NA
Company Name
DEN-MAT HOLDINGS, LLC
Labeler DUNS
809857704
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-22
Public Version
1
Public Version Date
2022-09-30
Public Version Status
New
Public Device Record Key
d76e64b8-c16e-40ef-bab1-1529677acdf0

Device Description

PERIOPTIX REP KIT US/CN

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
Yes
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
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)

GMDN Terms

Code Name
56318 LED dental light, battery-powered

Identifiers

Type ID
Primary D813AREPKITNA0

Customer Contacts

Phone
18004336628