Mepilex® Up

GUDID 07333350888848

Mepilex Up 20x50cm

Mölnlycke Health Care AB

Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 07333350888848
• NIH Device Record Key: c2a5a44f-b7f1-446a-9293-c187e00899f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepilex® Up
• Version Model Number: 212500
• Company DUNS: 631770658
• Company Name: Mölnlycke Health Care AB
• Device Count: 1
• DM Exempt: false
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	07333350315276 [Package]; Package: CASE [6 Units]; In Commercial Distribution
GS1	07333350341374 [Primary]
GS1	07333350888848 [Package]; Contains: 07333350341374; Package: PACK_OR_INNER_PACK [2 Units]; In Commercial Distribution

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: 2024-06-26
• Device Publish Date: 2024-06-18

On-Brand Devices [Mepilex® Up]

• 07333350679156: Mepilex Up, 10x20 cm US
• 07333350195625: Mepilex Up, 15x15 cm US
• 07333350364748: Mepilex Up, 10x10 cm US
• 07333350623074: Mepilex Up, 20x20 cm US
• 07333350888848: Mepilex Up 20x50cm
• 07333350293765: Mepilex Up 5x5cm