5450800040

GUDID 07613327289886

Lock Wrench

STRYER MEDTEC K.K.

Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system Soft-tissue ultrasonic surgical system
Primary Device ID07613327289886
NIH Device Record Key48b92216-9f94-45f9-9a6b-4be2b3a41b80
Commercial Distribution Discontinuation2017-03-14
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number5450800040
Catalog Number5450800040
Company DUNS690682147
Company NameSTRYER MEDTEC K.K.
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)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS107613327289886 [Primary]

FDA Product Code

MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


[07613327289886]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-23

Devices Manufactured by STRYER MEDTEC K.K.

07613327291827 - NA2020-01-06 Hyper Small Angled Handpiece without Tip, 25 kHz
07613327291957 - Hyper LT2020-01-06 Hard Tissue Curette Handpiece without Tip, 25 kHz
07613327289893 - Hyper LT2018-10-25 Angled Hard Tissue Curette Handpiece without Tip, 25 kHz
07613327291483 - NA2018-10-25 Torque Wrench, 1.96 Nm - 7 mm
07613327291490 - NA2018-10-25 Wrench, 10 mm
07613327291513 - NA2018-10-25 Step Torque Wrench, 7 mm
07613327291520 - NA2018-10-25 Step Torque Wrench, Offset, 7 mm
07613327291537 - NA2018-10-25 Cleaning Wire

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