FDA UDI In Commercial Distribution 🇺🇸 United States

Universal Base

DI: 05712821003607 · Model: 301240 · Elos Medtech Pinol A/S
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Universal Base
Primary DI
05712821003607
Version / Model
301240
Company Name
Elos Medtech Pinol A/S
Labeler DUNS
306155953
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-06
Public Version
1
Public Version Date
2021-10-14
Public Version Status
New
Public Device Record Key
d7839c9c-b9cd-439a-8a55-fee4d5f0704b

Device Description

The Universal Base is a titanium base designed to interface with a dental implant and to support a patient-specific multi-unit direct restoration cemented to the base. The base and the superstructure form a patient-specific abutment that will support a definitive multi-unit restoration.

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 05712821003607

Premarket Submissions

Submission Number Supplement Number
K201860 000