Primary Device ID | 00841036123888 |
NIH Device Record Key | 9922933c-dcda-43d0-ba2c-1b3d8bce1b60 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NEURO SYSTEM |
Version Model Number | 19-1000 |
Catalog Number | 19-1000 |
Company DUNS | 046189866 |
Company Name | BIOMET MICROFIXATION, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841036123888 [Primary] |
LRP | TRAY, SURGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841036123888]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-09-28 |
Device Publish Date | 2018-08-28 |
00841036197742 | 15-5010 |
00841036188054 | 15-5003 |
00841036187644 | 19-5006 |
00841036187637 | 15-5006 |
00841036187422 | 15-5000 |
00841036187415 | 19-5000 |
00841036182571 | 19-5002 |
00841036182564 | 19-5001 |
00841036182557 | 17-5000 |
00841036182540 | 17-5006 |
00841036182533 | 15-5002 |
00841036182526 | 15-5001 |
00841036123888 | 19-1000 |
00888233007320 | 19-5006 |
00888233007306 | 19-5002 |
00888233007269 | 19-5001 |
00888233007245 | 19-5000 |
00888233007207 | 17-5006 |
00888233007184 | 17-5000 |
00888233006934 | 15-5010 |
00888233006897 | 15-5006 |
00888233006828 | 15-5003 |
00888233006804 | 15-5002 |
00888233006767 | 15-5001 |
00888233006743 | 15-5000 |