398758

GUDID H6793987580

REDUCTION ATTACHMENT

SYNTHES (U.S.A.) LP

Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps
Primary Device IDH6793987580
NIH Device Record Key7df82216-6ac7-4639-927f-35ac43c4f3ba
Commercial Distribution StatusIn Commercial Distribution
Version Model Number398.758
Catalog Number398758
Company DUNS832637081
Company NameSYNTHES (U.S.A.) LP
Device Count1
DM Exempttrue
Pre-market Exempttrue
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
Phone+1(800)255-2500
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS110886982201614 [Primary]
HIBCCH6793987580 [Secondary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


[H6793987580]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2021-10-13
Device Publish Date2016-12-31

Devices Manufactured by SYNTHES (U.S.A.) LP

10886982305909 - NA2021-10-25 3.5MM DRILL SLEEVE
10886982308993 - NA2021-10-25 8MM CANNULATED STRAIGHT AWL WITH AO REAMER COUPLER
10886982309112 - NA2021-10-25 HANDLE
10886982309129 - NA2021-10-25 4.5 LCP PROTECTION SLEEVE
10886982309303 - NA2021-10-25 12MM CANNULATED DRILL BIT
10886982309310 - NA2021-10-25 13MM CANNULATED DRILL BIT
10886982311498 - NA2021-10-25 4.2MM CALIBRATED DRILL BIT
10886982311580 - NA2021-10-25 MEASURING DEVICE

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