Primary Device ID | 00841036062682 |
NIH Device Record Key | 0b3ebdc6-1c90-426f-8cfa-8998b5f20f51 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TOTAL MANDIBULAR SYSTEM |
Version Model Number | 24-1130 |
Catalog Number | 24-1130 |
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 | 00841036062682 [Primary] |
FZX | Guide, surgical, instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841036062682]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-11-22 |
Device Publish Date | 2018-08-28 |
00841036066826 | 24-1136 |
00841036062774 | 24-1135 |
00841036062682 | 24-1130 |
00841036062552 | 24-1131 |
00841036061432 | 24-1138 |
00841036065089 | 20-1300 |
00841036063573 | 24-4545 |
00841036063566 | 24-4544 |
00841036063467 | 24-2550 |
00841036063238 | 24-1302 |
00841036062842 | 24-2556 |
00841036062415 | 24-2400 |
00841036061852 | 24-2555 |
00841036061142 | 24-1308 |
00841036060824 | 24-2115 |
00841036060817 | 24-1306 |
00841036059279 | 24-2050 |