UD150L-40F

GUDID 04540217052134

SHIMADZU CORPORATION

Diagnostic x-ray system generator, stationary

• Primary Device ID: 04540217052134
• NIH Device Record Key: 12c9489d-e456-42c8-a52c-b9db9b917705
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UD150L-40F
• Version Model Number: 502-23373-58
• Company DUNS: 690558747
• Company Name: SHIMADZU CORPORATION
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04540217052134 [Primary]

FDA Product Code

• IZO: Generator, High-Voltage, X-Ray, Diagnostic

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: 2016-12-27

On-Brand Devices [UD150L-40F]

• 04540217052134: 502-23373-58
• 04540217018093: 502-23373-63
• 04540217018055: 502-23373-53