Mepilex® Border Post-Op

GUDID 07323190236718

Mepilex Border Post Op 6x8cm

Mölnlycke Health Care AB

Adhesive bandage

• Primary Device ID: 07323190236718
• NIH Device Record Key: 58f4d0ed-f82d-4d36-98a1-2210e13b2f98
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepilex® Border Post-Op
• Version Model Number: 496100
• 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
• 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 Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07323190154272 [Primary]
GS1	07323190236718 [Package]; Contains: 07323190236725; Package: CASE [8 Units]; In Commercial Distribution
GS1	07323190236725 [Package]; Contains: 07323190154272; Package: PACK_OR_INNER_PACK [10 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: 2024-01-31
• Device Publish Date: 2024-01-23

On-Brand Devices [Mepilex® Border Post-Op]

• 07323190183241: Mepilex Border Post-Op 4x8in/10x20cm, CVS
• 07323190282746: Mepilex Border Post Op 10x35cm
• 07323190236961: Mepilex Border Post Op 10x25cm
• 07323190236886: Mepilex Border Post Op 10x20cm
• 07323190236800: Mepilex Border Post Op 10x15cm
• 07323190237043: Mepilex Border Post Op 10x30cm
• 07323190236756: Mepilex Border Post Op 9x10cm
• 07323190236718: Mepilex Border Post Op 6x8cm
• 07333350949082: Mepilex Border Post Op 10x15cm
• 07333350312497: Mepilex Border Post-Op 6x8cm
• 07333350078133: Mepilex Border Post Op 9x10cm
• 07333350376345: Mepilex Border Post Op 10x35cm
• 07333350122089: Mepilex Border Post Op 10x30cm
• 07333350028336: Mepilex Border Post Op 10x20cm
• 07333350026943: Mepilex Border Post Op 10x25cm