Primary Device ID | 00887868267253 |
NIH Device Record Key | 1c5c2708-a325-4c8b-8ce2-ee63e0cb95a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OSS™ Orthopedic Salvage System |
Version Model Number | 151871 |
Catalog Number | 151871 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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 | 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)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868267253 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-04-27 |
Device Publish Date | 2018-11-13 |
00887868267253 | 151871 |
00887868267246 | 151870 |
00887868267239 | 151869 |
00887868267222 | 151868 |
00887868267215 | 151867 |
00887868267208 | 151866 |
00887868267192 | 151865 |
00887868267185 | 151864 |
00887868267178 | 151863 |
00887868267161 | 151862 |
00887868267154 | 151861 |
00887868251856 | CP102848 |
00887868251849 | CP102847 |
00887868251832 | CP102846 |
00887868251825 | CP102845 |
00887868251818 | CP102844 |
00887868251801 | CP102843 |
00887868251795 | CP102840 |
00887868251788 | CP102839 |
00887868251771 | CP102838 |