Pin Guide, Right

GUDID 00810111221894

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Treace Medical Concepts, Inc.

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 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 ID00810111221894
NIH Device Record Keybeadb290-3d64-47b2-ad84-e69c20237146
Commercial Distribution StatusIn Commercial Distribution
Brand NamePin Guide, Right
Version Model Number01-1000-014
Company DUNS054808082
Company NameTreace Medical Concepts, Inc.
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 Identifiers

Device Issuing AgencyDevice ID
GS100810111221894 [Primary]

FDA Product Code

FZXGuide, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


[00810111221894]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-21
Device Publish Date2023-11-13

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00810111221894Pin Guide, Right
00810111221870Pin Guide, Right

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