OrthoSolutions 'System26' Bone Screws

GUDID 05055662966350

VARISATION STAPLE HOLDER 90 DEG

ORTHO SOLUTIONS HOLDINGS LIMITED

Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Orthopaedic implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable
Primary Device ID05055662966350
NIH Device Record Keyfba4cb08-5c59-4d4e-9bdc-72959128ffc0
Commercial Distribution StatusIn Commercial Distribution
Brand NameOrthoSolutions 'System26' Bone Screws
Version Model NumberOS900092-NS
Company DUNS218648211
Company NameORTHO SOLUTIONS HOLDINGS LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
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+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com
Phone+441621843599
Emailquality@orthosol.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105055662966350 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


[05055662966350]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-21
Device Publish Date2021-01-13