352263S

GUDID H679352263S0

18.0MM REAMER HEAD-STERILE F/REAMER/IRRIGATOR/ASPIRATOR

Synthes GmbH

Medullary canal orthopaedic reamer, flexible
Primary Device IDH679352263S0
NIH Device Record Key04e51bed-d052-4078-8199-1c4a6fa3f8f1
Commercial Distribution StatusIn Commercial Distribution
Version Model Number352.263S
Catalog Number352263S
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
GS110886982194671 [Primary]
HIBCCH679352263S0 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTOREAMER

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-05-02
Device Publish Date2016-06-30

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10887587077062 - NA2024-08-29 MATRIXSTERNUM STRAIGHT PLATE 6 HOLES
10887587077079 - NA2024-08-29 MATRIXSTERNUM T-PLATE 7 HOLES
10887587077086 - NA2024-08-29 MATRIXSTERNUM X-PLATE SMALL/8 HOLES

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