BK-120MK

GUDID 04540217038428

SHIMADZU CORPORATION

Basic diagnostic x-ray system table, powered

• Primary Device ID: 04540217038428
• NIH Device Record Key: 01656d6a-4b5b-4e2b-8622-c115831ab21b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BK-120MK
• Version Model Number: 503-42580-22
• 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	04540217038428 [Primary]

FDA Product Code

• IXQ: Table, Radiographic, Stationary Top

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: 2016-09-16

On-Brand Devices [BK-120MK]

• 04540217056286: 566-19400-03
• 04540217038428: 503-42580-22
• 04540217064601: 566-19400-51