A7 Anesthesia System

GUDID 06944904039695

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Anaesthesia unit, mobile

• Primary Device ID: 06944904039695
• NIH Device Record Key: d3372ba8-4fe5-4e45-b06a-5986cd718541
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A7 Anesthesia System
• Version Model Number: A7
• Company DUNS: 654671304
• Company Name: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944904039695 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142552

FDA Product Code

• BSZ: Gas-Machine, Anesthesia

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-20

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

• 06903053046022 - Ventilator: 2025-12-08
• 06903053046060 - Ventilator: 2025-12-08
• 06903053081917 - Diagnostic Ultrasound System: 2025-12-08
• 06903053081924 - Diagnostic Ultrasound System: 2025-12-08
• 06903053081955 - Diagnostic Ultrasound System: 2025-12-08
• 06903053081962 - Diagnostic Ultrasound System: 2025-12-08
• 06903053081979 - Diagnostic Ultrasound System: 2025-12-08
• 06903053081986 - Diagnostic Ultrasound System: 2025-12-08