infinity OCTAGON TL WP Healing abutment GH 4.5 mm 5093733

GUDID E0HM50937331

Healing abutment GH 4.5 mm for infinity OCTAGON Dental Implant TL WP

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Screw endosteal dental implant, two-piece
Primary Device IDE0HM50937331
NIH Device Record Key10551531-1ea3-4630-b0dc-c8ebb2e7b860
Commercial Distribution StatusIn Commercial Distribution
Brand Nameinfinity OCTAGON TL WP Healing abutment GH 4.5 mm
Version Model Number5093733
Catalog Number5093733
Company DUNS318034329
Company NameHager & Meisinger Gesellschaft mit beschränkter Haftung
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com
Phone+1(508)588-3100
Emailkathystrange@acesurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCE0HM50937331 [Primary]
HIBCCE0HM50937339 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


[E0HM50937331]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-02-14
Device Publish Date2017-02-13

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