tenovi

GUDID 16978034830140

Shenzhen Jamr Medical Technology Co., Ltd.

Blood pressure cuff, reusable

• Primary Device ID: 16978034830140
• NIH Device Record Key: d3b25b47-c699-4d57-9b0f-20afbf79423c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: tenovi
• Version Model Number: Cuff 32-52CM
• Company DUNS: 421350239
• Company Name: Shenzhen Jamr Medical Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06978034830143 [Primary]
GS1	16978034830140 [Package]; Contains: 06978034830143; Package: [80 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K251331

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: 2025-12-22
• Device Publish Date: 2025-12-12

On-Brand Devices [tenovi]

• 16978034830140: Cuff 32-52CM
• 16978034830133: Cuff 15-28CM