PUREMED

GUDID 06951740517959

Shenzhen Jumper Medical Equipment Co.,Ltd.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 06951740517959
• NIH Device Record Key: c296e470-ff26-4e81-8f5b-1b2b04cb60aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PUREMED
• Version Model Number: JPD-HA200C
• Company DUNS: 529217911
• Company Name: Shenzhen Jumper Medical Equipment Co.,Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06951740517959 [Primary]

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2023-12-12
• Device Publish Date: 2023-12-04

Devices Manufactured by Shenzhen Jumper Medical Equipment Co.,Ltd.

• 06951740500654 - H-E-B inControl: 2023-12-14
• 06951740517959 - PUREMED: 2023-12-12
• 06951740517959 - PUREMED: 2023-12-12
• 06951740520133 - Jumper: 2023-11-28
• 06951740520140 - Jumper: 2023-11-28
• 06951740500647 - Misure: 2023-11-27
• 06951740500593 - JUMPER: 2023-11-13
• 06951740517904 - JUMPER: 2023-11-13
• 06951740500586 - JUMPER: 2023-11-08