M/DN® 00-2255-006-80

GUDID 00889024046221

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable
Primary Device ID00889024046221
NIH Device Record Keyd32f0eca-1f65-4ce7-8e54-421042f279eb
Commercial Distribution Discontinuation2017-05-19
Commercial Distribution StatusNot in Commercial Distribution
Brand NameM/DN®
Version Model Number2255-06-80
Catalog Number00-2255-006-80
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
GS100889024046221 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


[00889024046221]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-09-13
Device Publish Date2016-05-24

On-Brand Devices [M/DN®]

008890245817912255-26
008890245817842255-25
008890240466272255-36-80
008890240466032255-35-50
008890240465972255-34
008890240465802255-33-50
008890240465732255-33-37
008890240465662255-33-32
008890240465352255-32-37
008890240465282255-31-37
008890240464982255-28
008890240464812255-27
008890240464362255-20
008890240464292255-18
008890240464052255-16
008890240463992255-15-04
008890240463822255-15-03
008890240463752255-15-02
008890240463682255-15-01
008890240463442255-14
008890240463372255-13-01
008890240463202255-13
008890240463132255-12-50
008890240463062255-12-37
008890240462902255-12-33
008890240462832255-11
008890240462452255-07-50
008890240462382255-07-37
008890240462212255-06-80
008890240462142255-06-37
008890240461912255-05-80
008890240461842255-05-50
008890240461772255-05-32
008890240461602255-04-80
008890240461532255-04-50
008890240461462255-04-32
008890240461152255-03-03
008890240460612255-02-04
008890240460542255-02-02
008890240460472255-02-01
008890240458732254-300-13
008890240458662254-300-12
008890240458592254-300-11
008890240458422254-300-10
008890240458352254-300-09
008890240458282254-300-08
008890240458112254-300-07
008890240458042254-300-06
008890240457982254-285-13
008890240457812254-285-12

Trademark Results [M/DN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
M/DN
M/DN
75241965 2166590 Live/Registered
ZIMMER, INC
1997-02-14

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