Primary Device ID | 00887868041761 |
NIH Device Record Key | 623b1bd2-4bc0-4104-a090-d420e12775c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LOCKING CANCELLOUS SCREW |
Version Model Number | 8153-55-042 |
Catalog Number | 815355042 |
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 | 00887868041761 [Primary] |
HRS | PLATE, FIXATION, BONE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
Moist Heat or Steam Sterilization
[00887868041761]
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 |
00887868077449 | 815355014 |
00887868041808 | 8153-55-048 |
00887868041792 | 8153-55-046 |
00887868041778 | 8153-55-044 |
00887868041761 | 8153-55-042 |
00887868041747 | 8153-55-038 |
00887868041730 | 8153-55-036 |
00887868041716 | 8153-55-034 |
00887868041709 | 8153-55-032 |
00887868041686 | 8153-55-028 |
00887868041679 | 8153-55-026 |
00887868041655 | 8153-55-024 |
00887868041648 | 8153-55-022 |
00887868041631 | 8153-55-020 |
00887868041624 | 8153-55-018 |
00887868041617 | 8153-55-016 |