G7 ACETABULAR LINER 110017218

GUDID 00880304673496

Biomet Orthopedics, LLC

Non-constrained polyethylene acetabular liner
Primary Device ID00880304673496
NIH Device Record Key33f08a59-5c1e-4b5b-ba28-dbb0d0c8319c
Commercial Distribution StatusIn Commercial Distribution
Brand NameG7 ACETABULAR LINER
Version Model Number110017218
Catalog Number110017218
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
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)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304673496 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OQIHip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-11-02

On-Brand Devices [G7 ACETABULAR LINER]

00880304673571110017226
00880304673564110017225
00880304673557110017224
00880304673526110017221
00880304673519110017220
00880304673502110017219
00880304673496110017218
00880304673465110017215
00880304673458110017214
00880304673434110017212
00880304673427110017211
00880304673410110017210
00880304673403110017209
00880304673335110017199
00880304673311110017197
00880304673304110017196
00880304673298110017195
00880304673281110017194
00880304673274110017193
00880304673267110017192
00880304673250110017191
00880304673243110017190
00880304673236110017189
00880304673229110017188
00880304673212110017187
00880304673205110017186
00880304673199110017185
00880304673182110017184
00880304673175110017183
00880304673168110017182
00880304673151110017181
00880304673144110017180
00880304673137110017179
00880304673120110017178
00880304673113110017177
00880304673106110017176
00880304673090110017175
00880304528581010000988
00880304528574010000987
00880304528567010000986
00880304528550010000985
00880304528543010000984
00880304528536010000983
00880304528529010000982
00880304528512010000981
00880304528505010000980
00880304527232010000950
00880304527225010000949
00880304527218010000948
00880304527201010000946

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