BeneVision M12 Patient Monitor

GUDID 06936415975869

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

General-purpose multi-parameter bedside monitor

• Primary Device ID: 06936415975869
• NIH Device Record Key: b657dda1-b5c2-4e3b-9c7f-2dcdf0484404
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BeneVision M12 Patient Monitor
• Version Model Number: BeneVision M12
• Company DUNS: 654671304
• Company Name: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• 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	06936415975869 [Primary]

FDA Product Code

• MHX: Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

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: 2025-02-03
• Device Publish Date: 2025-01-24

On-Brand Devices [BeneVision M12 Patient Monitor]

• 06936415975876: BeneVision M12
• 06936415975869: BeneVision M12
• 06936415975357: BeneVision M12