Mepore® Film

GUDID 07323190295043

Unit pack Mepore Film 10x25 cm

Mölnlycke Health Care AB

Synthetic polymer semi-permeable film dressing, adhesive

• Primary Device ID: 07323190295043
• NIH Device Record Key: edd2f2f3-6c8a-415b-bf36-d3443c277611
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepore® Film
• Version Model Number: 272570
• 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	07323190295036 [Primary]
GS1	07323190295043 [Package]; Contains: 07323190295036; Package: PACK_OR_INNER_PACK [20 Units]; In Commercial Distribution
GS1	07323190295050 [Package]; Package: CASE [5 Units]; In Commercial Distribution

FDA Product Code

• NAD: Dressing, wound, occlusive

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: 2023-03-16
• Device Publish Date: 2023-03-08

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• 07332551950200: Normlgel Ag 45g
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• 07323190291892: Mepore Film 10x25 cm
• 07323190291960: Mepore Film 10x12 cm
• 07323190292042: Mepore Film 6x7 cm
• 07323190295104: Unit pack Mepore Film 15x20 cm
• 07323190295043: Unit pack Mepore Film 10x25 cm
• 07323190294992: Unit pack Mepore Film 10x12 cm
• 07323190294831: Unit pack Mepore Film 6x7cm
• 07333350722098: Unit pack Mepore Film 20x30 cm