FDA UDI In Commercial Distribution 🇺🇸 United States

EdgeEndo®

DI: 00818365026920 · Model: EE7004GP · US ENDODONTICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
60

Basic Information

Brand Name
EdgeEndo®
Primary DI
00818365026920
Version / Model
EE7004GP
Catalog Number
EE7004GP
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
92e89f96-0a13-481c-8ac3-2e7fdfc05c7c

Device Description

EdgeEndo .04 Gutta Percha Points™ 70

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 10818365026927
Primary 00818365026920

Customer Contacts

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