TRIWAY

GUDID 03760225718056

IN2BONES

Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment Orthopaedic implantation hammering attachment
Primary Device ID03760225718056
NIH Device Record Key5cba15c3-da33-47b9-93bd-86f63cc55ab0
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRIWAY
Version Model NumberN02 00024
Company DUNS263616749
Company NameIN2BONES
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

Device Identifiers

Device Issuing AgencyDevice ID
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]
GS103760225718056 [Primary]

FDA Product Code

FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument
FZXGuide, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


[03760225718056]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-17
Device Publish Date2020-06-09

On-Brand Devices [TRIWAY]

03760225717936N02 00009
03760225717899N02 00005
03760225717882N02 00004
03760225717875N02 00003
03760225717851N02 00001
03760225717615N20 ST211
03760225717585N20 ST201
03760225717974N02 00013
03760225717929N02 00008
03760225717912N02 00007
03760225718858G01 01641
03760225718834N02 00026
03760225718803N02 00021
03760225718797N02 00017
03760225718254G01 01591
03760225718230G01 40041
03760225718032N02 00016
03760225717998N02 00015
03760225717981N02 00014
03760225717905N02 00006
03760225718063N02 00025
03760225718056N02 00024
03760225718049N02 00023

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