Passive Abutment 011

GUDID 06009544017967

Passive Abutment, Engaging, for Ø5.0 Tri-Nex

SOUTHERN IMPLANTS (PTY) LTD

Dental implant suprastructure, permanent, preformed
Primary Device ID06009544017967
NIH Device Record Keyf8af50e7-6133-42b4-861c-1dabc5211eb9
Commercial Distribution StatusIn Commercial Distribution
Brand NamePassive Abutment
Version Model NumberPA-EL-50
Catalog Number011
Company DUNS636239584
Company NameSOUTHERN IMPLANTS (PTY) LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106009544017967 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

[06009544017967]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-11-08
Device Publish Date2019-01-08

On-Brand Devices [Passive Abutment]

06009544020585Vertical Passive Abutment, Engaging, for Ø3.0 IP Ex Hex
06009544020578Passive Abutment, Non-Engaging, for Ø3.0 IP Ex Hex
06009544020561Passive Abutment, Engaging, for Ø3.0 IP Ex Hex
06009544019817Vertical Passive Abutment, Non-Engaging, for Ø4.0 Ex Hex
06009544019800Vertical Passive Abutment, Engaging, for Ø4.0 Ex Hex
06009544019480Passive Abutment, Non-Engaging, for Ø4.0 Ex Hex
06009544019442Passive Abutment, Engaging, for Ø4.0 Ex Hex
06009544018247Passive Abutment, Non-Engaging, for Ø5.0 DC
06009544018230Passive Abutment, Non-Engaging, for Ø3.5 / Ø4.0 DC
06009544018223Passive Abutment, Non-Engaging, for Ø3.0 DC
06009544018162Passive Abutment for Ø4.8 Compact Conical
06009544017998Passive Abutment, Engaging, for Ø6.0 Tri-Nex
06009544017967Passive Abutment, Engaging, for Ø5.0 Tri-Nex
06009544017936Passive Abutment, Engaging, for Ø4.3 Tri-Nex
06009544017905Passive Abutment, Engaging, for Ø3.5 Tri-Nex
06009544017899Passive Abutment, Engaging, for Ø5.0 DC
06009544017882Passive Abutment, Engaging, for Ø3.5 / Ø4.0 DC
06009544017875Passive Abutment, Engaging, for Ø3.0 DC
06009544014072Passive Abutment, Non-Engaging, for IT Ø4.8 Interface
06009544014065Passive Abutment, Engaging, for IT Ø4.8 Interface
06009544013716Passive Abutment, Non-Engaging, for IT Ø6.5 Interface
06009544013709Passive Abutment, Engaging, for IT Ø6.5 Interface
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.