Primary Device ID | 00841036216498 |
NIH Device Record Key | 85e34af9-f12e-4dea-b881-7914e6f36f52 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STERNALOCK BLU SYSTEM |
Version Model Number | SP-3321 |
Catalog Number | SP-3321 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841036216498 [Primary] |
HRS | Plate, fixation, bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841036216498]
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 | 2016-10-14 |
00841036216511 | SP-3323 |
00841036184476 | SP-3192 |
00841036184469 | SP-3191 |
00841036183141 | SP-3184 |
00841036183134 | SP-3185 |
00841036179519 | SP-3143 |
00841036170257 | SP-3052 |
00841036216498 | SP-3321 |
00841036203696 | SP-3261 |
00841036196059 | SP-3245 |
00841036182502 | SP-3188 |
00841036177072 | SP-3142 |
00841036170080 | SP-3040 |
00841036169848 | SP-3037 |
00841036169763 | SP-3055 |
00841036158651 | SP-2914 |
00841036158644 | SP-2913 |
00841036155391 | SP-2891 |
00888233017619 | SP-3192 |
00888233017596 | SP-3191 |