FDA UDI Not in Commercial Distribution 🇺🇸 United States

3D Endo

DI: 00810126501356 · Model: KF2130 · 3D DENTAL DESIGNS AND DEVELOPMENT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3D Endo
Primary DI
00810126501356
Version / Model
KF2130
Catalog Number
KF2130
Company Name
3D DENTAL DESIGNS AND DEVELOPMENT, LLC
Labeler DUNS
080194935
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-20
Public Version
1
Public Version Date
2023-02-28
Public Version Status
New
Public Device Record Key
e2bcef79-10ab-454d-9fcc-c6a3645693e7
Distribution End Date
2023-02-20

Device Description

K-FILE Flex Type 21mm #30 6/Pk

Device Characteristics

Single Use
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EKS FILE, PULP CANAL, ENDODONTIC

GMDN Terms

Code Name
63720 Manual endodontic file/rasp, single-use

Identifiers

Type ID
Primary 00810126501356

Customer Contacts