NormaTec MVP Full Body Body Recovery Package 40344

GUDID 00817369021610

NormaTec MVP Recovery Package - Full Body Power Standard

NORMATEC INDUSTRIES LP

Intermittent venous compression system

• Primary Device ID: 00817369021610
• NIH Device Record Key: 16f9fa8b-d8c1-4d9d-9d83-b969d17f7898
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NormaTec MVP Full Body Body Recovery Package
• Version Model Number: NormaTec MVP Recovery Package - Full Body Power St
• Catalog Number: 40344
• 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	00817369021610 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112890

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: 2016-09-14

On-Brand Devices [NormaTec MVP Full Body Body Recovery Package]

• 00817369021627: NormaTec MVP Recovery Package - Full Body Power Tall
• 00817369021610: NormaTec MVP Recovery Package - Full Body Power Standard
• 00817369021603: NormaTec MVP Recovery Package - Full Body Power Short
• 00817369021597: NormaTec MVP Recovery Package - Full Body Short
• 00817369021580: NormaTec MVP Recovery Package - Full Body Tall
• 00817369021573: NormaTec MVP Recovery Package - Full Body Standard