FDA UDI In Commercial Distribution 🇺🇸 United States

EDENTA

DI: E312K8993140311 · Model: K899.314.031 · EDENTA ETABLISSEMENT
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
EDENTA
Primary DI
E312K8993140311
Version / Model
K899.314.031
Company Name
EDENTA ETABLISSEMENT
Labeler DUNS
448002915
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
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
bf8ef6ba-1db1-4d6f-88d0-184695034d04

Device Description

K-Diamond FG

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
DZP INSTRUMENT, DIAMOND, DENTAL

GMDN Terms

Code Name
16670 Diamond dental bur, reusable

Identifiers

Type ID
Unit of Use E312K899314031101
Primary E312K8993140311