Primary Device ID | 00880304516687 |
NIH Device Record Key | 2eb97240-2be5-437d-8e5b-ea1793fa0268 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TUNNELOC |
Version Model Number | 906512 |
Catalog Number | 906512 |
Company DUNS | 627100159 |
Company Name | Biomet Sports Medicine, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 | 00880304516687 [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 | 5 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2015-10-24 |
00880304516779 | 906515 |
00880304516755 | 906514 |
00880304516748 | 906513 |
00880304516687 | 906512 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() TUNNELOC 74528564 2034116 Live/Registered |
BIOMET U.S. RECONSTRUCTION, LLC 1994-05-24 |