Primary Device ID | 00887868000584 |
NIH Device Record Key | c2fc78a6-cc86-4acc-bc26-e12b7d3d29cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | END CAP |
Version Model Number | 1721 |
Catalog Number | 1721 |
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 | false |
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 | |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868000584 [Primary] |
HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
[00887868000584]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-22 |
Device Publish Date | 2015-10-24 |
00887868010750 | 1019-00-000 |
00887868000874 | 1805 |
00887868000591 | 1722 |
00887868000584 | 1721 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
END CAP 86961171 5077573 Live/Registered |
SKU LLC 2016-04-01 |
END CAP 73210897 1151747 Dead/Cancelled |
Tower Products, Inc. 1979-04-09 |