OCTAGON Infinity BL RC Basic screw, L 7.5 mm for cementable abutment 5022120

GUDID E0HM50221201

BL RC Basic screw, L 7.5 mm for cementable abutment for OCTAGON Infinity Dental Implant BL RC

Hager & Meisinger Gesellschaft mit beschränkter Haftung

Dental implant suprastructure, permanent, preformed
Primary Device IDE0HM50221201
NIH Device Record Keyfd8f6d93-46ac-4e70-9290-ad1a3cc8e7bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameOCTAGON Infinity BL RC Basic screw, L 7.5 mm for cementable abutment
Version Model Number5022120
Catalog Number5022120
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
HIBCCE0HM50221201 [Primary]
HIBCCXXXX50221209 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


[E0HM50221201]

Moist Heat or Steam Sterilization


Device Entry Metadata

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

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