1114-6004

GUDID 04546540172112

Spanner

Stryker Trauma GmbH

General internal orthopaedic fixation system implantation kit Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit
Primary Device ID04546540172112
NIH Device Record Keya4e1a826-1fde-4d05-821b-de2712728aed
Commercial Distribution StatusIn Commercial Distribution
Version Model Number1114-6004
Catalog Number1114-6004
Company DUNS330211587
Company NameStryker Trauma GmbH
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 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 Dimensions

Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter
Width12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540172112 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


[04546540172112]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-15
Device Publish Date2020-04-07

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