MXRUS2000

GUDID H679MXRUS20000

ROTARY MIXER

Synthes GmbH

Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer Bone matrix implant mixer
Primary Device IDH679MXRUS20000
NIH Device Record Keyeeaa029c-4c66-43c6-99cd-c71367aa152a
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberMXR-US-2000
Catalog NumberMXRUS2000
Company DUNS486711679
Company NameSynthes GmbH
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS107612335112995 [Direct Marking]
GS110886982001979 [Primary]
HIBCCH679MXRUS20000 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQVFILLER, BONE VOID, CALCIUM COMPOUND

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-04-28
Device Publish Date2015-09-14

Devices Manufactured by Synthes GmbH

10887587078359 - NA2024-04-16 MANDIBLE BODY REDUCTION HANDLE
10886982344427 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-11MM RIGID/TIBIAL FIXTN/LNG/STER
10886982344434 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-13MM RIGID/TIBIAL FIXTN/LNG/STER
10886982345745 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-11MM RIGID/LONG/STERILE
10886982345752 - NA2024-03-21 PROTECTION SLV F/NAILS/Ø8-13MM RIGID/LONG/STERILE
H67904038070S0 - TFN-ADVANCE2024-02-27 TFNA SCREW 70MM - STERILE
H6792161400 - NA2024-02-27 6.5MM CANCELLOUS BONE SCREW 16MM THREAD/140MM
H6792180750 - NA2024-02-27 6.5MM CANCELLOUS BONE SCREW FULLY THREADED/75MM

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