miniPhantom BS50-500

GUDID EIBABS505001

Solid Phantom, miniPhantom

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

• Primary Device ID: EIBABS505001
• NIH Device Record Key: 3ec21bed-6540-4c51-92a9-f2edf947d14e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: miniPhantom
• Version Model Number: BS50-500
• Catalog Number: BS50-500
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com
• Phone: +1 786 288 0369
• Email: service-usa@iba-group.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EIBABS505000 [Primary]
HIBCC	EIBABS505001 [Package]; Contains: EIBABS505000; Package: Carry Case [1 Units]; In Commercial Distribution

FDA Product Code

• IXG: Phantom, Anthropomorphic, Radiographic

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: 2023-04-20
• Device Publish Date: 2023-04-12

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