V80 Anesthetic Vaporizer

GUDID 06903053055000

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Desflurane anaesthesia vaporizer

• Primary Device ID: 06903053055000
• NIH Device Record Key: 149e9b7c-d1cd-4b96-93b5-f8a72f89cbd1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V80 Anesthetic Vaporizer
• Version Model Number: V80
• 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: false
• 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	06903053055000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240375

FDA Product Code

• CAD: Vaporizer, Anesthesia, Non-Heated

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: 2026-01-16
• Device Publish Date: 2026-01-08

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

• 06903053055000 - V80 Anesthetic Vaporizer: 2026-01-16
• 06903053055000 - V80 Anesthetic Vaporizer: 2026-01-16
• 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