FDA UDI In Commercial Distribution 🇺🇸 United States

ZERAMEX®

DI: 07640161390089 · Model: P15451 · Dentalpoint AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ZERAMEX®
Primary DI
07640161390089
Version / Model
P15451
Catalog Number
P15451
Company Name
Dentalpoint AG
Labeler DUNS
483229493
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-17
Public Version
5
Public Version Date
2023-02-06
Public Version Status
Update
Public Device Record Key
d7df5696-1545-48ec-a916-bc4ba2ef033f

Device Description

ZERAMEX®P VICARBO Screw SN Angular

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
PM Exempt
No
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
NHA ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 07640161390089

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152385 000
K163043 000