Mepilex® Border Sacrum

GUDID 07323190176748

Mepilex Border Sacrum 16x20cm BRU

Mölnlycke Health Care AB

Wound-nonadherent dressing, absorbent, non-antimicrobial

• Primary Device ID: 07323190176748
• NIH Device Record Key: 0ec55a93-98db-4093-b706-902b61f8ece4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepilex® Border Sacrum
• Version Model Number: 282055
• 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	07323190176731 [Package]; Package: CASE [5 Units]; In Commercial Distribution
GS1	07323190176748 [Package]; Contains: 07323190176755; Package: PACK_OR_INNER_PACK [10 Units]; In Commercial Distribution
GS1	07323190176755 [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: 2023-02-27
• Device Publish Date: 2023-02-18

On-Brand Devices [Mepilex® Border Sacrum]

• 07332430940612: Mepilex Border Sacrum 23x23 cm
• 07332430940599: Mepilex Border Sacrum 20x20cm
• 07332430940551: Mepilex Border Sacrum 18x18
• 07323190184170: Mepilex Border Heel 22x23cm
• 07323190038381: Mepilex Border Heel 18,5x24 cm
• 07323190176700: Mepilex Border Sacrum 22 x 25 cm BRU
• 07323190176748: Mepilex Border Sacrum 16x20cm BRU
• 07333350834074: Mepilex Border Sacrum, US 22 x 25 cm
• 07333350392451: Mepilex Border Sacrum, US 16x20cm