myQA®Daily

GUDID EIBAE30631001

myQA Daily Device

IBA Dosimetry GmbH

Accelerator system quality assurance device

• Primary Device ID: EIBAE30631001
• NIH Device Record Key: 119e295d-334d-403b-b01c-9dee6ecd64fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myQA®Daily
• Version Model Number: E3063100
• Company DUNS: 332599307
• Company Name: IBA Dosimetry GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: +49912860738
• Email: service@iba-group.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EIBAE30631000 [Primary]
HIBCC	EIBAE30631001 [Package]; Contains: EIBAE30631000; Package: Carry Case [1 Units]; In Commercial Distribution

FDA Product Code

• LHO: Instrument, Quality-Assurance, Radiologic

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: 2019-05-03
• Device Publish Date: 2019-04-25

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• EIBAE20703000 - DOSE-X: 2023-04-21 DOSE-X Dosimeter BNC