Primary Device ID | 00889024631892 |
NIH Device Record Key | bbc793b3-31fd-4329-8e20-a48fc20c8f3d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Persona® The Personalized Knee® OsseoTi® |
Version Model Number | 42-5350-064-02 |
Catalog Number | 42-5350-064-02 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 |
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 | 00889024631892 [Primary] |
MBH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-01 |
Device Publish Date | 2022-11-23 |
00889024632011 | 42-5350-088-02 |
00889024632004 | 42-5350-088-01 |
00889024631991 | 42-5350-083-02 |
00889024631984 | 42-5350-083-01 |
00889024631977 | 42-5350-079-02 |
00889024631960 | 42-5350-079-01 |
00889024631953 | 42-5350-075-02 |
00889024631946 | 42-5350-075-01 |
00889024631939 | 42-5350-071-02 |
00889024631922 | 42-5350-071-01 |
00889024631915 | 42-5350-067-02 |
00889024631908 | 42-5350-067-01 |
00889024631892 | 42-5350-064-02 |
00889024631885 | 42-5350-064-01 |
00889024631878 | 42-5350-061-02 |
00889024631861 | 42-5350-061-01 |
00889024631854 | 42-5350-058-02 |
00889024631847 | 42-5350-058-01 |
00889024646414 | 42-5405-000-41 |
00889024646407 | 42-5405-000-38 |
00889024646391 | 42-5405-000-35 |
00889024646384 | 42-5405-000-32 |
00889024646377 | 42-5405-000-29 |