PHYSICA ZUK 9061.20.061

GUDID 08033390128650

Tibial EM Guide Slope Adjuster

LIMACORPORATE SPA

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID08033390128650
NIH Device Record Key8381a9ed-9cf6-4c78-b68a-f22d11bbc7f3
Commercial Distribution StatusIn Commercial Distribution
Brand NamePHYSICA ZUK
Version Model Number9061.20.061
Catalog Number9061.20.061
Company DUNS432066322
Company NameLIMACORPORATE SPA
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
GS108033390128650 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


[08033390128650]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-11
Device Publish Date2022-08-03

On-Brand Devices [PHYSICA ZUK]

08033390128667Tibial EM Guide Height Adjuster
08033390128650Tibial EM Guide Slope Adjuster
08033390128643Tibial EM Guide Ankle Clamp

Trademark Results [PHYSICA ZUK]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PHYSICA ZUK
PHYSICA ZUK
79187846 not registered Dead/Abandoned
LIMACORPORATE S.P.A.
2016-01-27

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