Primary Device ID | 00819824023894 |
NIH Device Record Key | 91e54f16-afbe-489c-831b-56f0a9d87b59 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XULTAN CROSSLINK DRIVER REMOVAL TOOL |
Version Model Number | 30290316 |
Catalog Number | 30290316 |
Company DUNS | 080474650 |
Company Name | MET 1 TECHNOLOGIES, 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 | false |
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 | 9154726762 |
yone@met1tech.com | |
Phone | 9154726762 |
yone@met1tech.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00819824023894 [Primary] |
NKB | Thoracolumbosacral Pedicle Screw System |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00819824023894]
Moist Heat or Steam Sterilization
[00819824023894]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-03-29 |
00819824023894 | THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLANT DEVICE MANUFACTURED FROM TITANIUM AND SILICONE |
00819824023757 | THE XULTAN 5.5 PEDICLE SCREW SYSTEM IS AN IMPLANT DEVICE MANUFACTURED FROM TITANIUM AND SILICONE |