Joimax® Intracs® EM Patient Tracker

GUDID 04250337116585

Joimax GmbH

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• Primary Device ID: 04250337116585
• NIH Device Record Key: ed202e10-2cfd-4a7c-a04d-14cd22efd4b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Joimax® Intracs® EM Patient Tracker
• Version Model Number: JINTPT2235
• 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337116585 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192663

FDA Product Code

• OLO: Orthopedic Stereotaxic Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-22
• Device Publish Date: 2021-11-12

Devices Manufactured by Joimax GmbH

• 04250337100737 - Flatscreen: 2024-05-03 joimax® Flatscreen Monitor 19.0'' TFT
• 04250337100744 - trolley: 2024-05-03 joimax® Monitor Trolley, grey
• 04250337105473 - Flatscreen: 2024-05-03 Flatscreen Monitor 24.0'' TFT
• 04250337106340 - Flatscreen: 2024-05-03 joimax® Flatscreen Monitor 42.0'' TFT
• 04250337109396 - Flatscreen: 2024-05-03 joimax® Flatscreen Monitor 24.0'' TFT
• 04250337114345 - Flatscreen: 2024-05-03 joimax® Flatscreen Monitor 32,0'' TFT
• 04250337114376 - Monitor: 2024-05-03 joimax® Flatscreen 26,0'' TFT
• 04250337117353 - Monitor: 2024-05-03 joimax® Touch Monitor 21,5“ TFT