Primary Device ID | 00887868056703 |
NIH Device Record Key | 941802d6-b273-47d0-9505-344c1c5ed898 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CANNULATED CORTICAL LAG SCREW |
Version Model Number | 8514-48-146 |
Catalog Number | 851448146 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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 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 | 00887868056703 [Primary] |
HTN | WASHER, BOLT NUT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00887868007705 | 14250-70 |
00887868007699 | 14250-65 |
00887868007682 | 14250-60 |
00887868007675 | 14250-55 |
00887868007668 | 14250-50 |
00887868007651 | 14250-48 |
00887868007644 | 14250-46 |
00887868007637 | 14250-44 |
00887868007620 | 14250-42 |
00887868007613 | 14250-40 |
00887868007606 | 14250-38 |
00887868007590 | 14250-36 |
00887868007583 | 14250-34 |
00887868007576 | 14250-32 |
00887868007569 | 14250-30 |
00887868056765 | 8514-48-170 |
00887868056758 | 8514-48-165 |
00887868056741 | 8514-48-160 |
00887868056734 | 8514-48-155 |
00887868056727 | 8514-48-150 |
00887868056710 | 8514-48-148 |
00887868056703 | 8514-48-146 |
00887868056697 | 8514-48-144 |
00887868056680 | 8514-48-142 |
00887868056673 | 8514-48-140 |
00887868056666 | 8514-48-138 |
00887868056659 | 8514-48-136 |
00887868056642 | 8514-48-134 |
00887868056635 | 8514-48-132 |
00887868056628 | 8514-48-130 |