C6-2 Ultrasonic Probe(FDA)

GUDID 06944904091105

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 06944904091105
• NIH Device Record Key: b19e0c1c-3f85-4662-ac26-ba7c4a795ec8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: C6-2 Ultrasonic Probe(FDA)
• Version Model Number: 120-004591-00
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944904091105 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182636

FDA Product Code

• ITX: Transducer, Ultrasonic, Diagnostic

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: 2019-12-23
• Device Publish Date: 2019-12-14

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