Primary Device ID | 00887868139123 |
NIH Device Record Key | c7b115b2-69f4-4fc8-9de5-f1a32a5c572a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TWIST- OFFSCREW |
Version Model Number | 110018500 |
Catalog Number | 110018500 |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868139123 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868139123]
Moist Heat or Steam Sterilization
[00887868139123]
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 |
00887868139239 | 110018511 |
00887868139222 | 110018510 |
00887868139215 | 110018509 |
00887868139208 | 110018508 |
00887868139192 | 110018507 |
00887868139185 | 110018506 |
00887868139178 | 110018505 |
00887868139161 | 110018504 |
00887868139154 | 110018503 |
00887868139147 | 110018502 |
00887868139130 | 110018501 |
00887868139123 | 110018500 |
00887868139116 | 110018499 |
00887868139109 | 110018498 |
00887868139093 | 110018488 |
00887868139086 | 110018487 |
00887868139079 | 110018486 |
00887868139062 | 110018485 |