Primary Device ID | 00841036011314 |
NIH Device Record Key | 0f79993e-2a59-431a-bc41-72d3b9364916 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXTERNAL DISTRACTION SYSTEM |
Version Model Number | 01-5918 |
Catalog Number | 01-5918 |
Company DUNS | 046189866 |
Company Name | BIOMET MICROFIXATION, INC |
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(904)741-4400 |
FXJAX-ORDERS@ZIMMERBIOMET.COM | |
Phone | +1(904)741-4400 |
FXJAX-ORDERS@ZIMMERBIOMET.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841036011314 [Primary] |
HTY | PIN, FIXATION, SMOOTH |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841036011314]
Moist Heat or Steam Sterilization
[00841036011314]
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 | 2015-11-25 |
00841036057435 | 99-3582 |
00841036057428 | 99-3581 |
00841036057411 | 99-3575 |
00841036057404 | 99-3572 |
00841036057398 | 99-3570 |
00841036010942 | 01-3587 |
00841036010935 | 01-3586 |
00841036010928 | 01-3585 |
00841036010911 | 01-3584 |
00841036010904 | 01-3580 |
00841036010850 | 01-3552 |
00841036010843 | 01-3551 |
00841036072650 | 99-5924 |
00841036070885 | 99-5918 |
00841036066796 | 99-5926 |
00841036011338 | 01-5926 |
00841036011321 | 01-5924 |
00841036011314 | 01-5918 |