CERAGEM Master V6

GUDID 08809494000099

CERAGEM Co., Ltd.

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• Primary Device ID: 08809494000099
• NIH Device Record Key: 42b37d0e-0ca1-4b77-9b4f-dd7496bbd0fb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CERAGEM Master V6
• Version Model Number: CGM MB-1702
• Company DUNS: 688326136
• Company Name: CERAGEM Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	08809494000099 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K202937
• Premarket Notification: K220572

FDA Product Code

• JFB: Table, Physical Therapy, Multi Function

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: 2021-04-08
• Device Publish Date: 2021-03-31

On-Brand Devices [CERAGEM Master V6]

• 08809494000099: CGM MB-1702
• 08809494000082: CGM MB-1701