Invia Motion 60 Days Bundle

GUDID 10020451454082

This new SKU will contain: Motion 60 Days (101011596 / 0874014) - 1x15 pack of medium foam dressings (101011863 / 0876226) - 2x5 packs of motion 150ml canisters (101011598 / 0874016) - 1 return shipping box for the Motion 60 Day (101029404 / 0874004SB).

MEDELA, INC.

Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set Negative-pressure wound therapy system dressing set

• Primary Device ID: 10020451454082
• NIH Device Record Key: 3925d21a-eec9-421c-9957-1045d265f462
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Invia Motion 60 Days Bundle
• Version Model Number: 101045408
• Company DUNS: 052002029
• Company Name: MEDELA, INC.
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	10020451454082 [Primary]

FDA Product Code

• OMP: Negative Pressure Wound Therapy Powered Suction Pump

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-02-28
• Device Publish Date: 2023-02-20

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