FDA UDI In Commercial Distribution 🇺🇸 United States

EDENTA

DI: E3126516101 · Model: 6516-10 · EDENTA ETABLISSEMENT
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
EDENTA
Primary DI
E3126516101
Version / Model
6516-10
Company Name
EDENTA ETABLISSEMENT
Labeler DUNS
448002915
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-02-03
Public Version
1
Public Version Date
2022-02-11
Public Version Status
New
Public Device Record Key
3a4cbb67-c83d-408c-9649-f47959f221ed

Device Description

HeadMaster Passive-cylindrical

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EBL PIN, RETENTIVE AND SPLINTING, AND ACCESSORY INSTRUMENTS

GMDN Terms

Code Name
38609 Root canal post, preformed

Identifiers

Type ID
Unit of Use E312651610101
Primary E3126516101