MG II® 00-5125-011-17

GUDID 00889024186910

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00889024186910
NIH Device Record Keye8829211-09e7-4807-8245-1b30a7055e55
Commercial Distribution StatusIn Commercial Distribution
Brand NameMG II®
Version Model Number5125-11-17
Catalog Number00-5125-011-17
Company DUNS056038268
Company NameZimmer, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com
Phone+1(800)348-2759
Emailzimmer.consumerrelations@zimmerbiomet.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024186910 [Primary]

FDA Product Code

HWEINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


[00889024186910]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-22
Device Publish Date2016-12-22

On-Brand Devices [MG II®]

008890241870165125-84
008890241870095125-81
008890241869965125-60
008890241869275125-11-18
008890241869105125-11-17
008890241869035125-11-16
008890241868975125-11-15
008890241868805125-11-14
008890241868735125-11-13
008890241868665125-11-12
008890241868595125-11-11
008890241868425125-11-10
008890241868355125-10-09
008890241868115120-87
008890241868045120-85
008890241867985120-83
008890241866205120-67
008890241866135120-61
008890241865905120-53
008890241865835120-52-01
008890241865525120-08
008890244360605110-53-23
008890244358415110-23-20
008890244358345110-23-17
008890244357975110-23-09
008890241866375120-69
008890241866065120-54
008890241865455110-75-60
008890241865385110-75-55
008890241865215110-75-50
008890241865145110-75-45
008890241865075110-75-40
008890241864915110-75-35
008890241864845110-75-30
008890241864775110-75-25
008890241864605110-75-20
008890241864535110-70-60
008890241864465110-70-55
008890241864395110-70-50
008890241864225110-70-45
008890241864155110-70-40
008890241864085110-70-35
008890241863925110-70-30
008890241863855110-70-25
008890241863785110-70-20
008890244360465110-53-17
008890245826995110-53-09
008890244360535110-53-20
008890244360395110-53-15
008890244360225110-53-13

Trademark Results [MG II]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MG II
MG II
74144880 1677487 Live/Registered
ZIMMER, INC.
1991-03-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.