Mepore®

GUDID 07323190254637

Mepore 9x25cm

Mölnlycke Health Care AB

Adhesive bandage

• Primary Device ID: 07323190254637
• NIH Device Record Key: dd1c0110-7a71-47ad-bbe9-e876bb71c4eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepore®
• Version Model Number: 671200
• Company DUNS: 631770658
• Company Name: Mölnlycke Health Care AB
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com
• Phone: +46737733775
• Email: pedro.lopes@molnlycke.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07323190254637 [Package]; Contains: 07323190254644; Package: CASE [7 Units]; In Commercial Distribution
GS1	07323190254644 [Package]; Contains: 07323190254866; Package: PACK_OR_INNER_PACK [30 Units]; In Commercial Distribution
GS1	07323190254866 [Primary]

FDA Product Code

• NAC: Dressing, wound, hydrophilic

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: 2022-10-31
• Device Publish Date: 2022-10-21

On-Brand Devices [Mepore®]

• 07323190254798: Mepore 10x11 cm
• 07323190254705: Mepore 9x30cm
• 07323190254637: Mepore 9x25cm
• 07323190196388: Mepore 6x7cm
• 07323190196418: Mepore 9x10cm
• 07323190254750: Mepore 9x35cm
• 07323190254385: Mepore 9x15cm OTC Norden
• 07332430675125: Mepore Roll 7cmx5m
• 07332430675088: Mepore Roll 4cmx5m
• 07323190254545: Mepore 9x20cm