BK-200

GUDID 04540217039654

SHIMADZU CORPORATION

Basic diagnostic x-ray system table, powered

• Primary Device ID: 04540217039654
• NIH Device Record Key: e425091c-79d3-4d82-9bcb-e97f5a0dd719
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BK-200
• Version Model Number: 503-61750-42
• 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	04540217039654 [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: 2016-10-03

On-Brand Devices [BK-200]

• 04540217052530: 566-16400-65
• 04540217052523: 566-16400-05
• 04540217047581: 566-16400-86
• 04540217047574: 566-16400-85
• 04540217047567: 566-16400-81
• 04540217047550: 566-16400-80
• 04540217039715: 503-61750-48
• 04540217039685: 503-61750-45
• 04540217039654: 503-61750-42
• 04540217039623: 503-61750-36
• 04540217039593: 503-61750-32
• 04540217060900: 566-16400-82
• 04540217062706: 563-16400-87
• 04540217062591: 566-16404-50
• 04540217062539: 563-61750-81