Pulse Full Body Recovery Package 40144

GUDID 00817369021115

Pulse Recovery Package - Full Body Power Standard

NORMATEC INDUSTRIES LP

Sequential venous compression system

• Primary Device ID: 00817369021115
• NIH Device Record Key: cc5c1bef-8d6c-4c8b-974d-c2f60b8c4f96
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pulse Full Body Recovery Package
• Version Model Number: Pulse Recovery Package - Full Body Power Standard
• Catalog Number: 40144
• Company DUNS: 111448069
• Company Name: NORMATEC INDUSTRIES LP
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817369021115 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160608

FDA Product Code

• IRP: Massager, Powered Inflatable Tube

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-13

On-Brand Devices [Pulse Full Body Recovery Package]

• 00817369021122: Pulse Recovery Package - Full Body Power Tall
• 00817369021115: Pulse Recovery Package - Full Body Power Standard
• 00817369021108: Pulse Recovery Package - Full Body Power Short
• 00817369021092: Pulse Recovery Package - Full Body Short
• 00817369021085: Pulse Recovery Package - Full Body Tall
• 00817369021078: Pulse Recovery Package - Full Body Standard