Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries PMDBPA

GUDID 05060488570933

Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries

PROACTIVE MEDICAL PRODUCTS, LLC

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 05060488570933
• NIH Device Record Key: 96e2ea9b-8c5d-4eae-be94-c1a4ce4a7480
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries
• Version Model Number: PMDBPA
• Catalog Number: PMDBPA
• Company DUNS: 078582655
• Company Name: PROACTIVE MEDICAL PRODUCTS, LLC
• 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: 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

Customer Support Contacts

• Phone: +1 855 237 7622
• Email: sales@proactivemedical.com

Device Dimensions

• Length: 6 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060488570933 [Primary]
GS1	05060488571015 [Package]; Package: Carton [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K150545

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: 2020-01-09
• Device Publish Date: 2020-01-01

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