AEQUALIS REVERSED FRACTURE

GUDID 03700386931901

TORNIER

Total reverse shoulder prosthesis
Primary Device ID03700386931901
NIH Device Record Key44887de2-0958-4ca7-83c9-74dd589cabdf
Commercial Distribution StatusIn Commercial Distribution
Brand NameAEQUALIS REVERSED FRACTURE
Version Model NumberDWD922
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 Batchfalse
Serial Numbertrue
Manufacturing Datefalse
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
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 Identifiers

Device Issuing AgencyDevice ID
GS103700386931901 [Primary]

FDA Product Code

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

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-06-03
Device Publish Date2015-10-16

On-Brand Devices [AEQUALIS REVERSED FRACTURE]

03700386936401DWD978
03700386936395DWD977
03700386936388DWD976
03700386936371DWD968
03700386936364DWD967
03700386936357DWD966
03700386932618DWD972
03700386932601DWD971
03700386932595DWD970
03700386931901DWD922
03700386931888DWD920
03700386931871DWB010
03700386932106DWD953
03700386932090DWD934
03700386932083DWD952
03700386932076DWD933
03700386932069DWD951
03700386932052DWD932
03700386932045DWD931
03700386932038DWD905
03700386932021DWD904
03700386932014DWD903
03700386932007DWD902
03700386931994DWD901
03700386972836RETENTIVE TRIAL INSERT
03700386972829RETENTIVE TRIAL INSERT
03700386972812RETENTIVE TRIAL INSERT
03700386972805HUMERAL TRIAL INSERT
03700386972799HUMERAL TRIAL INSERT
03700386972782HUMERAL TRIAL INSERT
03700386972744RETENTIVE TRIAL INSERT
03700386972737RETENTIVE TRIAL INSERT
03700386972720RETENTIVE TRIAL INSERT
03700386972713HUMERAL SPACER TRIAL
03700386972706HUMERAL TRIAL STEM
03700386972690HUMERAL TRIAL STEM
03700386972683HUMERAL TRIAL STEM
03700386972676HUMERAL TRIAL STEM
03700386972669HUMERAL TRIAL STEM
03700386972447HUMERAL LUG FOR HEIGHT GAUGE
03700386972416HEIGHT GAUGE
03700386972409Prosthesis Holder
03700386972393Diaphysis Reamer
03700386972386Diaphysis Reamer
03700386972379Diaphysis Reamer
03700386972362Diaphysis Reamer
03700386972355Diaphysis Reamer
03700386972348Nut (Prosthesis Holder)
03700386971846Wrench for Plug and Union Screw
03700386971235HUMERAL TRIAL INSERT

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