MatriXX Evolution kalibriert

GUDID EIBAE30300121

MatriXX Evolution kalibriert

IBA Dosimetry GmbH

Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device Accelerator system quality assurance device

• Primary Device ID: EIBAE30300121
• NIH Device Record Key: ced7d872-3aa7-4a55-acd3-30f0870cde68
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MatriXX Evolution kalibriert
• Version Model Number: E3030012
• Company DUNS: 332599307
• Company Name: IBA Dosimetry 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com
• Phone: +1 901 386-2242
• Email: USService@iba-group.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EIBAE30300120 [Primary]
HIBCC	EIBAE30300121 [Package]; Contains: EIBAE30300120; Package: Aluminium case [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072374

FDA Product Code

• IYE: Accelerator, Linear, Medical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-09

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