Shoulder iD MWJ006

GUDID 03700434023701

BLUEPRINT Primary Reversed Glenoid Guide

TORNIER

Orthopaedic prosthesis implantation positioning instrument, single-use
Primary Device ID03700434023701
NIH Device Record Key6d120d9d-a94e-4726-82b8-ce635e25c6a6
Commercial Distribution StatusIn Commercial Distribution
Brand NameShoulder iD
Version Model NumberMWJ006
Catalog NumberMWJ006
Company DUNS260324876
Company NameTORNIER
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com
Phone+330476613500
Emailorder@tornier.com

Device Dimensions

Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter
Outer Diameter29 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103700434023701 [Primary]

FDA Product Code

KWSPROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-31
Device Publish Date2024-05-23

On-Brand Devices [Shoulder iD]

03700434023732BLUEPRINT Primary Reversed Bone Model
03700434023725BLUEPRINT Primary Reversed Glenoid Guide
03700434023718BLUEPRINT Primary Reversed Glenoid Guide
03700434023701BLUEPRINT Primary Reversed Glenoid Guide
03700434023695BLUEPRINT Primary Reversed Glenoid Guide

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