M/DN® 00-2252-260-10

GUDID 00889024041677

Zimmer, Inc.

Femur nail, sterile Femur nail Femur nail Femur nail Femur nail Femur nail Femur nail Femur nail Femur nail
Primary Device ID00889024041677
NIH Device Record Keybffe97fe-31d0-4b08-8c2e-7e320a213edc
Commercial Distribution StatusIn Commercial Distribution
Brand NameM/DN®
Version Model Number2252-260-10
Catalog Number00-2252-260-10
Company DUNS056038268
Company NameZimmer, Inc.
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 Datetrue
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

Device Dimensions

Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter
Device Size Text, specify0
Length26 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024041677 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSBROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-08-12
Device Publish Date2015-09-24

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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