Avance 66499-00

GUDID 07332551967499

Mölnlycke Health Care AB

Negative-pressure wound therapy system drape

• Primary Device ID: 07332551967499
• NIH Device Record Key: 6f20cc21-e2d7-43ff-b0c6-98281b7f07bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Avance
• Version Model Number: 66499
• Catalog Number: 66499-00
• Company DUNS: 631770658
• Company Name: Mölnlycke Health Care AB
• Device Count: 80
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07332551924072 [Unit of Use]
GS1	07332551967499 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-10-28

On-Brand Devices [Avance]

• 07332551967499: 66499
• 07323190160570: 773014-00
• 07323190160532: 773013-00
• 07323190160495: 772013-00
• 07323190154432: 772009-00
• 07323190154395: 772003-00
• 07323190193752: 662752-01
• 07323190193684: 662652-01
• 07323190193660: 662552-01
• 07323190193639: 662452-01
• 07323190193592: 664352-01
• 07323190193578: 664252-01
• 07323190193530: 664152-01
• 07323190193516: 662352-01
• 07323190193486: 662252-01
• 07323190193448: 662152-01