NormaTec MVP Pro Recovery Package 40405

GUDID 00817369021689

MVP Pro Recovery Package - Power Tall

NORMATEC INDUSTRIES LP

Intermittent venous compression system Intermittent venous compression system Intermittent venous compression system

• Primary Device ID: 00817369021689
• NIH Device Record Key: e5c20cc6-11f7-4b72-827a-9d7cdab2da9c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NormaTec MVP Pro Recovery Package
• Version Model Number: MVP Pro Recovery Package - Power Tall
• Catalog Number: 40405
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817369021689 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013436

FDA Product Code

• JOW: Sleeve, Limb, Compressible

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 Pro Recovery Package]

• 00817369021689: MVP Pro Recovery Package - Power Tall
• 00817369021672: MVP Pro Recovery Package - Power Standard
• 00817369021665: MVP Pro Recovery Package - Power Short
• 00817369021658: MVP Pro Recovery Package - Short
• 00817369021641: MVP Pro Recovery Package - Tall
• 00817369021634: MVP Pro Recovery Package - Standard