Primary Device ID | 00887868342066 |
NIH Device Record Key | 0de5a3dd-c98e-4003-bd5b-29769c688b4f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Regenerex® Ringloc®+ Hip System |
Version Model Number | PT-116046 |
Catalog Number | PT-116046 |
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 | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com | |
Phone | +1(800)348-9500 |
customerservice@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 | 00887868342066 [Primary] |
MBL | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-26 |
Device Publish Date | 2019-04-18 |
00887868342165 | PT-116066 |
00887868342158 | PT-116064 |
00887868342141 | PT-116062 |
00887868342134 | PT-116060 |
00887868342127 | PT-116058 |
00887868342110 | PT-116056 |
00887868342103 | PT-116054 |
00887868342097 | PT-116052 |
00887868342080 | PT-116050 |
00887868342073 | PT-116048 |
00887868342066 | PT-116046 |
00887868342059 | PT-116044 |
00887868342042 | PT-116042 |
00887868342035 | PT-106080 |
00887868342028 | PT-106078 |
00887868342011 | PT-106076 |
00887868342004 | PT-106074 |
00887868341991 | PT-106072 |
00887868341984 | PT-106070 |
00887868341977 | PT-106068 |
00887868341960 | PT-106066 |
00887868341953 | PT-106064 |
00887868341946 | PT-106062 |
00887868341939 | PT-106060 |
00887868341922 | PT-106058 |
00887868341915 | PT-106056 |
00887868341908 | PT-106054 |
00887868341892 | PT-106052 |
00887868341885 | PT-106050 |
00887868341878 | PT-106048 |
00887868341861 | PT-106046 |
00887868341854 | PT-106044 |
00887868341847 | PT-104072 |
00887868341830 | PT-104066 |
00887868341823 | PT-104064 |
00887868341816 | PT-104062 |
00887868341809 | PT-104060 |
00887868341793 | PT-104058 |
00887868341786 | PT-104056 |
00887868341779 | PT-104054 |
00887868341762 | PT-104052 |
00887868341755 | PT-104050 |
00887868341748 | PT-104048 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() REGENEREX 78753529 3331701 Live/Registered |
Biomet Manufacturing, LLC 2005-11-14 |