Primary Device ID | 00887868006586 |
NIH Device Record Key | 8f4f365d-3610-445d-92ec-56fb6a3d0c7b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CANNULATED CANCELLOUS SCREW |
Version Model Number | 14192-90 |
Catalog Number | 1419290 |
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 |
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 | 00887868006586 [Primary] |
LXT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
[00887868006586]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00887868010095 | 14192-120 |
00887868010088 | 14192-115 |
00887868010071 | 14192-110 |
00887868010064 | 14192-105 |
00887868010057 | 14192-100 |
00887868006593 | 14192-95 |
00887868006586 | 14192-90 |
00887868006579 | 14192-85 |
00887868006562 | 14192-80 |
00887868006555 | 14192-75 |
00887868006548 | 14192-70 |
00887868006531 | 14192-65 |
00887868006524 | 14192-60 |
00887868006517 | 14192-55 |
00887868006500 | 14192-50 |
00887868006494 | 14192-45 |
00887868006487 | 14192-40 |
00887868006470 | 14192-35 |