BeneVision N12 OR Patient Monitor

GUDID 06936415985462

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

General-purpose multi-parameter bedside monitor

• Primary Device ID: 06936415985462
• NIH Device Record Key: 39bf0419-ff78-4eb8-b1f2-3c4cf5b2cf2c
• Commercial Distribution Discontinuation: 2024-12-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: BeneVision N12 OR Patient Monitor
• Version Model Number: BeneVision N12 OR
• 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	06936415985462 [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: 2024-12-19
• Device Publish Date: 2024-12-11

Devices Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

• 06936415904661 - MR Na/K Check Solution: 2026-02-02
• 06936415904678 - MR Detergent Solution: 2026-02-02
• 06936415904685 - MR Buffer Solution: 2026-02-02
• 06944904084459 - Chemistry Analyzer: 2026-02-02
• 06903053010641 - M-30CFL LYSE: 2026-01-30
• 06936415908805 - M-30CFL LYSE: 2026-01-30
• 06936415908812 - M-30CFL LYSE: 2026-01-30
• 06936415994457 - PROBE CLEANSER: 2026-01-30