Primary Device ID | 00889024670679 |
NIH Device Record Key | 083db978-5834-44b0-b92f-45c9711db022 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HGPII Acetabular Component |
Version Model Number | 32-6732-93-01 |
Catalog Number | 32-6732-093-01 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com | |
Phone | +1(800)348-2759 |
zimmer.consumerrelations@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024670679 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-13 |
Device Publish Date | 2024-11-05 |