E9-4 Ultrasonic Probe(FDA) 84002-40

GUDID 06936415902780

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Rectal/vaginal ultrasound imaging transducer

• Primary Device ID: 06936415902780
• NIH Device Record Key: 97c4ebea-3f23-430f-825a-f488697c0c7b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: E9-4 Ultrasonic Probe(FDA) 84002-40
• Version Model Number: Z103-40
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +8675581888998
• Email: service@mindray.com.cn

Device Identifiers

Device Issuing Agency	Device ID
GS1	06936415902780 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171891

FDA Product Code

• ITX: Transducer, Ultrasonic, Diagnostic

Sterilization

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

[06936415902780]

Liquid Chemical

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-17
• Device Publish Date: 2018-07-17

On-Brand Devices [E9-4 Ultrasonic Probe(FDA) 84002-40]

• 06944904092133: Z103-40
• 06936415902780: Z103-40