Primary Device ID | 00887868275791 |
NIH Device Record Key | 3efadefc-5f41-45a0-a068-6b441cd77e75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spine System |
Version Model Number | LV01488 |
Catalog Number | LV01488 |
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 | 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 |
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 | 00887868275791 [Primary] |
NKB | Thoracolumbosacral pedicle screw system |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
[00887868275791]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-03-11 |
Device Publish Date | 2019-02-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SPINE SYSTEM 74164936 1732796 Live/Registered |
AESCULAP AG. 1991-05-09 |
SPINE SYSTEM 74164935 1864032 Live/Registered |
AESCULAP AG. 1991-05-09 |