Distraction Tube - Right LV01291

GUDID 00880304855403

DISTRACTION TUBE - RIGHT

Highridge Medical, LLC

Orthopaedic surgical procedure kit, non-medicated, reusable
Primary Device ID00880304855403
NIH Device Record Key676999d2-517d-45ec-abf1-c4d0bae686f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameDistraction Tube - Right
Version Model NumberLV01291
Catalog NumberLV01291
Company DUNS119260394
Company NameHighridge Medical, LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com
Phone+1(800)447-3625
Emailusbrocustomerservice@highridgemedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304855403 [Primary]

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


[00880304855403]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-07
Device Publish Date2025-04-29

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