HGPII Acetabular Component 32-6732-091-01

GUDID 00889024670655

Zimmer, Inc.

Non-constrained polyethylene acetabular liner
Primary Device ID00889024670655
NIH Device Record Key5aab5d29-e288-4c63-a630-883730d8fce9
Commercial Distribution StatusIn Commercial Distribution
Brand NameHGPII Acetabular Component
Version Model Number32-6732-91-01
Catalog Number32-6732-091-01
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 Datetrue
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
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
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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 Identifiers

Device Issuing AgencyDevice ID
GS100889024670655 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPHPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-13
Device Publish Date2024-11-05

On-Brand Devices [HGPII Acetabular Component]

0088902467068632-6732-94-01
0088902467067932-6732-93-01
0088902467066232-6732-92-01
0088902467065532-6732-91-01
0088902467064832-6732-90-01
0088902467063132-6732-89-01
0088902467062432-6732-88-01
0088902467061732-6732-87-01
0088902467060032-6732-14-01
0088902467059432-6732-13-01
0088902467058732-6732-12-01
0088902467057032-6732-11-01
0088902467056332-6732-10-01
0088902467055632-6732-09-01
0088902467054932-6732-08-01
0088902467053232-6732-07-01
0088902467052532-6732-06-01
0088902467051832-6732-05-01
0088902467050132-6728-94-01
0088902467049532-6728-93-01
0088902467048832-6728-92-01
0088902467047132-6728-91-01
0088902467046432-6728-90-01
0088902467045732-6728-89-01
0088902467044032-6728-88-01
0088902467043332-6728-87-01
0088902467042632-6728-86-01
0088902467041932-6728-85-01
0088902467040232-6728-14-01
0088902467039632-6728-13-01
0088902467038932-6728-12-01
0088902467037232-6728-11-01
0088902467036532-6728-10-01
0088902467035832-6728-09-01
0088902467034132-6728-08-01
0088902467033432-6728-07-01
0088902467032732-6728-06-01
0088902467031032-6728-05-01
0088902467030332-6728-04-01
0088902467029732-6728-03-01
0088902467028032-6726-05-01
0088902467027332-6726-04-01
0088902467026632-6726-03-01
0088902467025932-6726-02-01
0088902467024232-6722-83-01
0088902467023532-6722-82-01
0088902467022832-6722-21-01
0088902467021132-6722-03-01
0088902467020432-6722-02-01
0088902467019832-6722-01-01

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