Bar Phantom 243-955

GUDID 00718175009550

Bar Phantom, Cardiac, High Resolution

BIODEX MEDICAL SYSTEMS, INC.

Nuclear medicine phantom, test object

• Primary Device ID: 00718175009550
• NIH Device Record Key: a20e269e-85e4-49a4-b166-42295f3b22c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bar Phantom
• Version Model Number: 243-955
• Catalog Number: 243-955
• Company DUNS: 043833813
• Company Name: BIODEX MEDICAL SYSTEMS, 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00718175009550 [Primary]

FDA Product Code

• JAR: Phantom, Test-Pattern, Radionuclide

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: 2018-02-15

On-Brand Devices [Bar Phantom]

• 00718175009871: Bar Phantom, Symbia, 21" X 16"
• 00718175009550: Bar Phantom, Cardiac, High Resolution
• 00718175009352: Bar Phantom, Rectangular
• 00718175008164: Bar Phantom, GE
• 00718175004395: Bar Phantom, Symbia and E-Cam
• 00718175003985: Bar Phantom, E CAM, 4-Quadrant
• 00718175003800: Bar Phantom, Standard, High Resolution