maidesite

GUDID 06975960551371

Zhejiang Mateside Medical Devices Technology Co., Ltd

Body/limb elastic exerciser

• Primary Device ID: 06975960551371
• NIH Device Record Key: 79d0e271-1dbe-4ce5-920c-bbc2c8fd2dd6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: maidesite
• Version Model Number: EN11
• Company DUNS: 699411523
• Company Name: Zhejiang Mateside Medical Devices Technology Co., Ltd
• 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: true
• Serial Number: false
• 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	06975960551371 [Primary]

FDA Product Code

• BXB: Exerciser, Powered

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: 2025-04-03
• Device Publish Date: 2025-03-26

Devices Manufactured by Zhejiang Mateside Medical Devices Technology Co., Ltd

• 06975960550527 - VOCIC: 2025-05-27
• 06975960551395 - VOCIC: 2025-05-08
• 06975960551388 - VOCIC: 2025-05-07
• 06975960558394 - VOCIC: 2025-04-09
• 06975960551371 - maidesite: 2025-04-03
• 06975960551371 - maidesite: 2025-04-03
• 06975960551326 - VOCIC: 2025-01-16
• 06975960551333 - VOCIC: 2025-01-16
• 06975960551340 - VOCIC: 2025-01-16