Standard Imaging MIMI Phantom 91240

GUDID 00850019946512

Standard Imaging MIMI (Multiple Imaging Modality Isocentricity) Phantom is designed for daily or weekly quality assurance of the geometric accuracy of the isocenter described by several systems included on many modern linear accelerators: the positioning lasers, the kV imaging system, the MV treatment beam and for Elekta and Varian optical guidance systems as well.

STANDARD IMAGING INC.

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• Primary Device ID: 00850019946512
• NIH Device Record Key: 421255cb-2d72-4423-9a29-eadfc13dd147
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Standard Imaging MIMI Phantom
• Version Model Number: 91240
• Catalog Number: 91240
• Company DUNS: 788084705
• Company Name: STANDARD IMAGING INC.
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850019946512 [Primary]

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: 2023-06-30
• Device Publish Date: 2023-06-22

Devices Manufactured by STANDARD IMAGING INC.

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• 00850019946093 - Standard Imaging SuperMAX Electrometer: 2023-06-30 Standard Imaging SuperMAX Electrometer is a 2-channel electrometer designed to be connected to a radiation detector, (ionization
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