FDA UDI In Commercial Distribution 🇺🇸 United States

EDENTA

DI: E31281IK2060301 · Model: 81IK.206.030 · EDENTA ETABLISSEMENT
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EDENTA
Primary DI
E31281IK2060301
Version / Model
81IK.206.030
Company Name
EDENTA ETABLISSEMENT
Labeler DUNS
448002915
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
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
125311c8-9897-461f-8ceb-a5947143ea04

Device Description

Surgical cutters IK

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
EJL BUR, DENTAL

GMDN Terms

Code Name
16668 Carbide dental bur, reusable

Identifiers

Type ID
Primary E31281IK2060301