VADER Pedicle System, K-wire, Nitinol, Ø 1.1 × 472 mm 42-542

GUDID 07640172552094

VADER Pedicle System, K-wire, Nitinol, Ø 1.1 × 472 mm

icotec AG

Orthopaedic bone wire Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable Spinal intraoperative positioning pin, reusable
Primary Device ID07640172552094
NIH Device Record Keyff59314b-827a-4fb4-92f3-ddf58f464120
Commercial Distribution StatusIn Commercial Distribution
Brand NameVADER Pedicle System, K-wire, Nitinol, Ø 1.1 × 472 mm
Version Model Number42-542
Catalog Number42-542
Company DUNS480789465
Company Nameicotec AG
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+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch

Device Identifiers

Device Issuing AgencyDevice ID
GS107640172552094 [Primary]

FDA Product Code

NKBThoracolumbosacral Pedicle Screw System

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


[07640172552094]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-02-19
Device Publish Date2023-01-13

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07640164848822 - icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 55 mm2024-04-04 icotec Pedicle System 6.0, Screw, Ti, Polyaxial, Ø 8.5 x 55 mm

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