AGK16150

GUDID 07613252257905

Kirschner Wire / L, Tips trocar / smooth

Stryker Trauma SA

Orthopaedic bone wire Orthopaedic bone wire Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use Orthopaedic intraoperative positioning pin, single-use
Primary Device ID07613252257905
NIH Device Record Keya5b00d03-2594-4928-8f70-be01af04eec7
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberAGK16150
Catalog NumberAGK16150
Company DUNS481999654
Company NameStryker Trauma SA
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0
Length150 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS107613252257905 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


[07613252257905]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-02-11
Device Publish Date2020-02-03

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