Primary Device ID | 00887868008566 |
NIH Device Record Key | 1eb2a09f-1e92-4289-8c9b-f3471657fc63 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SOLID CANCELLOUS LAG SCREW, PARTIAL THREAD |
Version Model Number | 14374-55 |
Catalog Number | 1437455 |
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 | 00887868008566 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868008566]
Moist Heat or Steam Sterilization
[00887868008566]
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 |
00887868008573 | 14374-60 |
00887868008566 | 14374-55 |
00887868008559 | 14374-50 |
00887868008542 | 14374-45 |
00887868008535 | 14374-40 |
00887868008528 | 14374-35 |
00887868008511 | 14374-30 |
00887868008504 | 14374-28 |
00887868008498 | 14374-26 |
00887868008481 | 14374-24 |
00887868008474 | 14374-22 |
00887868008467 | 14374-20 |
00887868008450 | 14374-18 |
00887868008443 | 14374-16 |
00887868008436 | 14374-14 |
00887868008429 | 14374-12 |
00887868008412 | 14374-10 |