Primary Device ID | 03662663080835 |
NIH Device Record Key | 3c25e120-0bdd-4099-987b-1cc4cca6ac04 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | The Tether™ |
Version Model Number | 240H6003 |
Catalog Number | 240H6003 |
Company DUNS | 119260394 |
Company Name | Highridge Medical, 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 | false |
OTC Over-The-Counter | false |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com | |
Phone | +1(800)447-3625 |
usbrocustomerservice@highridgemedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03662663080835 [Primary] |
QHP | Vertebral body tethering system |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
[03662663080835]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-02-14 |
Device Publish Date | 2025-02-06 |
03662663080842 | Tether Tension Indicator |
03662663080835 | Tether Reel Tensioner |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() THE TETHER 88637747 not registered Live/Pending |
Zimmer Biomet Spine, Inc. 2019-10-01 |