miniPhantom R

GUDID EIBABS550001

miniPhantom R used as Patient QA Phantom with MatriXX Resolution

IBA Dosimetry GmbH

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• Primary Device ID: EIBABS550001
• NIH Device Record Key: 067881cb-7d79-4a94-8e43-a12a076c368f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: miniPhantom R
• Version Model Number: BS55000
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EIBABS550000 [Primary]
HIBCC	EIBABS550001 [Package]; Contains: EIBABS550000; 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: 2021-05-26
• Device Publish Date: 2021-05-18

On-Brand Devices [miniPhantom R]

• EIBAM10900001: miniPhantom R used as Patient QA Phantom with MatriXX Resolution
• EIBABS550001: miniPhantom R used as Patient QA Phantom with MatriXX Resolution