Intracs® JINTST23

GUDID 04250337118046

joimax® Intracs® EM Navigation Sensor Tray 230

Joimax GmbH

Electromagnetic surgical navigation device tracking system

• Primary Device ID: 04250337118046
• NIH Device Record Key: b02150b4-710b-4773-afd3-691f7c07429b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Intracs®
• Version Model Number: JINTST23
• Catalog Number: JINTST23
• Company DUNS: 344267187
• Company Name: Joimax GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337118046 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192663

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

[04250337118046]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-09-18
• Device Publish Date: 2022-12-30

On-Brand Devices [Intracs®]

• 04250337117834: Intracs® em Sensor Tools DIN container, black
• 04250337118046: joimax® Intracs® EM Navigation Sensor Tray 230
• 04250337118039: joimax® Intracs® EM Navigation Sensor Tray 180
• 04250337118022: joimax® Intracs® EM Navigation Sensor Tray 150