G7® Vivacit-E® 30113205

GUDID 00889024520141

Zimmer, Inc.

Non-constrained polyethylene acetabular liner
Primary Device ID00889024520141
NIH Device Record Key47f35ac8-a0d1-4836-b31c-b83a7ebaf917
Commercial Distribution StatusIn Commercial Distribution
Brand NameG7® Vivacit-E®
Version Model Number30113205
Catalog Number30113205
Company DUNS056038268
Company NameZimmer, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024520141 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDIProsthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-01-08
Device Publish Date2019-12-31

On-Brand Devices [G7® Vivacit-E®]

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0088902452087530154010
0088902452086830154009
0088902452085130154008
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0088902452081330153609
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0088902452079030153607
0088902452078330153606
0088902452077630153605
0088902452076930153604
0088902452075230153208
0088902452074530153207
0088902452073830153206
0088902452072130153205
0088902452071430153204
0088902452070730153203
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0088902452067730152806
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0088902452052330123609
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0088902452050930123607
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0088902452047930123604
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0088902452045530123207
0088902452044830123206
0088902452043130123205
0088902452042430123204
0088902452041730123203
0088902452040030123202

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