Primary Device ID | 05019279343225 |
NIH Device Record Key | 8073a52f-7e8e-478e-9fd6-964049d7ea75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MALLORY/HEAD REVISION HIP SYSTEM |
Version Model Number | 104911 |
Catalog Number | 104911 |
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.c |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05019279343225 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00880304441750 | 104917 |
00880304189942 | 104817 |
00880304189935 | 104816 |
00880304189928 | 104815 |
00880304189904 | 104814 |
00880304189881 | 104813 |
00880304189850 | 104811 |
00880304189836 | 104810 |
00880304189812 | 104809 |
00880304005334 | 104812 |
05019279343263 | 104915 |
05019279343256 | 104914 |
05019279343249 | 104913 |
05019279343232 | 104912 |
05019279343225 | 104911 |
05019279343218 | 104910 |