FDA UDI In Commercial Distribution 🇺🇸 United States

EdgeOne™

DI: 10818365021632 · Model: 8806387801184_1 · US ENDODONTICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
60

Basic Information

Brand Name
EdgeOne™
Primary DI
10818365021632
Version / Model
8806387801184_1
Catalog Number
8806387801184_1
Company Name
US ENDODONTICS, LLC
Labeler DUNS
061317427
Distribution Status
In Commercial Distribution
Device Count in Pkg
60
Record Status
Published
Publish Date
2023-06-25
Public Version
1
Public Version Date
2023-07-03
Public Version Status
New
Public Device Record Key
e4b0a70b-abbd-4aa8-acab-c121a3fb6230

Device Description

Classic Fit EdgeOne™ Gutta Percha Points Medium

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKM GUTTA-PERCHA

GMDN Terms

Code Name
45081 Synthetic gutta-percha

Identifiers

Type ID
Unit of Use 20818365021639
Primary 10818365021632

Customer Contacts

Phone
+1(423)283-0047 ext. 103