Primary Device ID | 00880304453265 |
NIH Device Record Key | 1f797f80-ccd5-48d3-927c-e1b7ac0288ff |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ToggleLoc |
Version Model Number | 904720 |
Catalog Number | 904720 |
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 | 00880304453265 [Primary] |
JDR | STAPLE, 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 | 2020-05-11 |
Device Publish Date | 2015-10-24 |
00880304463905 | 909846 |
00880304453333 | 904727 |
00880304453326 | 904726 |
00880304453319 | 904725 |
00880304453302 | 904724 |
00880304453296 | 904723 |
00880304453289 | 904722 |
00880304453272 | 904721 |
00880304453265 | 904720 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TOGGLELOC 90570421 not registered Live/Pending |
Biomet Manufacturing, LLC 2021-03-10 |