Primary Device ID | 00887868251818 |
NIH Device Record Key | bf7c186a-cb87-4ba8-9327-85c28e01c0e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OSS™ Orthopedic Salvage System |
Version Model Number | CP102844 |
Catalog Number | CP102844 |
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 | 00887868251818 [Primary] |
KRO | PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-05-29 |
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 |