A3 Anesthesia System

GUDID 06944904055091

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Anaesthesia unit, mobile

• Primary Device ID: 06944904055091
• NIH Device Record Key: c6e44290-338f-4272-b9b4-76ef04049b95
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: A3 Anesthesia System
• Version Model Number: A3
• 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	06944904055091 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123211

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

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