Primary Device ID | 00887868106583 |
NIH Device Record Key | 0d394b25-c145-4350-b5d7-a1ea66c5dac3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OSSEOTI RECONSTRUCTIVE SYSTEM |
Version Model Number | 110003827 |
Catalog Number | 110003827 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Phone | +1(800)348-9500 |
customerservice@zimmerbiomet.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887868106583 [Primary] |
HWC | Screw, fixation, bone |
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 |
00887868130939 | 110003784 |
00887868130922 | 110003772 |
00887868130915 | 110003760 |
00887868106590 | 110003831 |
00887868106583 | 110003827 |
00887868106576 | 110003821 |
00887868106569 | 110003819 |
00887868106552 | 110003815 |
00887868106545 | 110003809 |
00887868106538 | 110003807 |
00887868106521 | 110003803 |
00887868106514 | 110003797 |
00887868106507 | 110003794 |
00887868106491 | 110003790 |
00887868106484 | 110003786 |
00887868106477 | 110003782 |
00887868106460 | 110003778 |
00887868106453 | 110003774 |
00887868106446 | 110003770 |
00887868106439 | 110003766 |
00887868106422 | 110003762 |