Mepore® Film & Pad

GUDID 07323190294923

Unit Pack Mepore Film & Pad 9x15 cm

Mölnlycke Health Care AB

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• Primary Device ID: 07323190294923
• NIH Device Record Key: d09a36c7-a50f-4785-9812-b6f2cd3697c3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepore® Film & Pad
• Version Model Number: 275500
• 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	07323190294725 [Primary]
GS1	07323190294923 [Package]; Contains: 07323190294725; Package: PACK_OR_INNER_PACK [30 Units]; In Commercial Distribution
GS1	07323190294930 [Package]; Package: CASE [8 Units]; In Commercial Distribution
GS1	07333350408565 [Package]; Contains: 07333350847265; Package: CASE [8 Units]; In Commercial Distribution
GS1	07333350847265 [Package]; Contains: 07323190294725; Package: PACK_OR_INNER_PACK [30 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: 2024-02-07
• Device Publish Date: 2024-01-30

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• 07333350180621: Unit Pack Mepore Film & Pad 9x25 cm
• 07333350498641: Unit Pack Mepore Film & Pad 9x20 cm
• 07333350696986: Unit Pack Mepore Film & Pad 5x7 cm, oval
• 07333350070755: Unit pack Mepore Film & Pad 9x35 cm
• 07323190294923: Unit Pack Mepore Film & Pad 9x15 cm
• 07333350046767: Unit Pack Mepore Film & Pad 5x7 cm, square
• 07323190291045: Unit Pack Mepore Film & Pad 4x5 cm
• 07333350105587: Unit Pack Mepore Film& Pad 9x30 cm