OCTAGON Infinity BL RC ALLIGATOR Abutment GH 4.0 mm 5022127

GUDID E0HM50221271

BL RC ALLIGATOR Abutment GH 4.0 mm for OCTAGON Infinity Dental Implant BL RC

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Dental implant suprastructure, permanent, preformed
Primary Device IDE0HM50221271
NIH Device Record Key516bf040-370a-4b1a-b427-a1b5930b6aa5
Commercial Distribution StatusIn Commercial Distribution
Brand NameOCTAGON Infinity BL RC ALLIGATOR Abutment GH 4.0 mm
Version Model Number5022127
Catalog Number5022127
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCE0HM50221271 [Primary]
HIBCCXXXX50221279 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


[E0HM50221271]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2016-09-09

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