Primary Device ID | 00880304973206 |
NIH Device Record Key | f2d2081b-9269-4bc2-881a-c2b6cf338736 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Polaris™ 6.35 Spinal System |
Version Model Number | 14-501045 |
Catalog Number | 14-501045 |
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 | 00880304973206 [Primary] |
KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
[00880304973206]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-01 |
Device Publish Date | 2020-06-23 |