FDA UDI Not in Commercial Distribution 🇺🇸 United States

Viteo Base Ti

DI: 07615208323085 · Model: 689595 · IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Viteo Base Ti
Primary DI
07615208323085
Version / Model
689595
Catalog Number
689595
Company Name
IVOCLAR VIVADENT AKTIENGESELLSCHAFT
Labeler DUNS
448015938
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-29
Public Version
2
Public Version Date
2025-01-30
Public Version Status
Update
Public Device Record Key
05522fe4-90c3-4017-a2a9-7584b5b25f34
Distribution End Date
2025-01-29

Device Description

Viteo Screw BI-OC 3.4/4.1/5.0/6.0

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 07615208323085
Previous DIVO6895951