Primary Device ID | 00887868310829 |
NIH Device Record Key | e30441c7-02bd-48a0-95c8-0a98a2432089 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biomet® Hip System |
Version Model Number | 163704 |
Catalog Number | 163704 |
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 | 00887868310829 [Primary] |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIOMET 79083976 not registered Dead/Abandoned |
VEOLIA WATER TECHNOLOGIES ITALIA S.p.A. 2010-03-23 |
BIOMET 78703978 3176481 Live/Registered |
ZIMMER, INC. 2005-08-31 |
BIOMET 78498921 3235830 Dead/Cancelled |
ARKEMA, INC. 2004-10-13 |
BIOMET 75282520 2301253 Live/Registered |
ZIMMER, INC. 1997-04-10 |
BIOMET 74722414 not registered Dead/Abandoned |
NOREL, S.A. 1995-08-29 |
BIOMET 73585352 1411822 Live/Registered |
BIOMET, INC. 1986-02-28 |
BIOMET 73165517 1153792 Live/Registered |
BIOMET, INC. 1978-04-07 |