Mepilex® Border Flex Lite

GUDID 00050428250341

Mepilex Border Flex Lite 7,5x7,5cm, CVS

Mölnlycke Health Care AB

Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 00050428250341
• NIH Device Record Key: 4be40bfe-e520-42e0-b3e1-a6400ecf9184
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepilex® Border Flex Lite
• Version Model Number: 581288
• 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	00050428250341 [Package]; Contains: 07333350066550; Package: PACK_OR_INNER_PACK [3 Units]; In Commercial Distribution
GS1	07333350066550 [Primary]
GS1	07333350381608 [Package]; Package: CASE [14 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: 2023-12-29
• Device Publish Date: 2023-12-21

On-Brand Devices [Mepilex® Border Flex Lite]

• 07323190249084: Mepilex Border Flex Lite 15x15cm
• 07323190249008: Mepilex Border Flex Lite 5x12,5cm
• 07333350157418: Mepilex Border Flex Lite 10x10cm
• 07333350912772: Mepilex Border Flex Lite 4x5cm
• 07333350382476: Mepilex Border Flex Lite 7,5x7,5cm
• 07333350551346: Mepilex Border Flex Lite 10x10cm, OTC US
• 07333350515904: Mepilex Border Flex Lite 5x12,5cm, OTC US
• 07333350399870: Mepilex Border Flex Lite 4x5cm, OTC US
• 07333350389048: Mepilex Border Flex Lite 7,5x7,5cm, OTC US
• 00050428436332: Mepilex Border Flex Lite 5x12,5cm, CVS
• 00050428433713: Mepilex Border Flex Lite 4x5cm, CVS
• 00050428250341: Mepilex Border Flex Lite 7,5x7,5cm, CVS
• 00050428435939: Mepilex Border Flex Lite 10x10cm, CVS