CUFF

GUDID 06944904003931

Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Blood pressure cuff, reusable

• Primary Device ID: 06944904003931
• NIH Device Record Key: 61d002d1-6de5-47a9-a222-41c68c1c99c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CUFF
• Version Model Number: 0010-30-12160
• 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: true
• Serial Number: false
• 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

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	06944904003931 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191769

FDA Product Code

• DXQ: Blood Pressure Cuff

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: 2020-05-07
• Device Publish Date: 2020-04-29

On-Brand Devices [CUFF]

• 06944904003931: 0010-30-12160
• 06944904059587: 0683-15-0007-0
• 06944904059570: 0683-15-0006-01
• 06944904059563: 0683-15-0005-01
• 06944904059556: 0683-15-0004-01
• 06944904059549: 0683-15-0003-01
• 06944904059532: 0683-15-0002-01
• 06944904059525: 0683-15-0001-01