CERAGEM Master V7

GUDID 08809494000983

CERAGEM Co., Ltd.

Massage table/couch, line-powered

• Primary Device ID: 08809494000983
• NIH Device Record Key: 41a2b187-e3d1-45a6-871a-f91522fdaa57
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CERAGEM Master V7
• Version Model Number: CGM MB-2302
• 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	08809494000983 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243644

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: 2025-02-20
• Device Publish Date: 2025-02-12

On-Brand Devices [CERAGEM Master V7]

• 08809494000983: CGM MB-2302
• 08809494000686: CGM MB-2301