Primary Device ID | 00887868316104 |
NIH Device Record Key | 0774ab3b-bf49-4a31-b8e4-5af297a5e467 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vital™ |
Version Model Number | 805M7530 |
Catalog Number | 805M7530 |
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 |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com | |
Phone | +1(800)447-3625 |
USBROCustomerService@zimmerbiomet.com |
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 | 00887868316104 [Primary] |
NKB | Thoracolumbosacral pedicle screw system |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
[00887868316104]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-07 |
Device Publish Date | 2019-10-30 |