FDA UDI In Commercial Distribution 🇺🇸 United States

Max

DI: D76815882K0 · Model: 15882K · KEYSTONE DENTAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Max
Primary DI
D76815882K0
Version / Model
15882K
Company Name
KEYSTONE DENTAL, INC.
Labeler DUNS
787471015
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-26
Public Version
3
Public Version Date
2021-03-31
Public Version Status
Update
Public Device Record Key
6cc25dad-cf0f-46ce-8822-7e0e6299f638

Device Description

Healing Abutment

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE IMPLANT, ENDOSSEOUS, ROOT-FORM

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary D76815882K0

Customer Contacts