Primary Device ID | 00880304830325 |
NIH Device Record Key | 8900ba85-c1ee-4dc7-90fb-fe1ce5891742 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TIMBERLINE MPF LATERAL MODULAR PLATE FIXATION SYSTEM |
Version Model Number | 8616-4516 |
Catalog Number | 8616-4516 |
Company DUNS | 018577570 |
Company Name | BIOMET SPINE LLC |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304830325 [Primary] |
OVD | Intervertebral fusion device with integrated fixation, lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
[00880304830325]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2016-10-14 |