Mepore® Film

GUDID 07323190292042

Mepore Film 6x7 cm

Mölnlycke Health Care AB

Synthetic polymer semi-permeable film dressing, adhesive

• Primary Device ID: 07323190292042
• NIH Device Record Key: 63364bca-a7aa-441d-8e55-ab4640e44542
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepore® Film
• Version Model Number: 270600
• Company DUNS: 631770658
• Company Name: Mölnlycke Health Care AB
• Device Count: 1
• DM Exempt: true
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	07323190292035 [Package]; Package: CASE [6 Units]; In Commercial Distribution
GS1	07323190292042 [Package]; Contains: 07323190292981; Package: PACK_OR_INNER_PACK [100 Units]; In Commercial Distribution
GS1	07323190292981 [Primary]

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: 2022-11-04
• Device Publish Date: 2022-10-27

On-Brand Devices [Mepore® Film]

• 07332551950200: Normlgel Ag 45g
• 07323190291823: Mepore Film 15x20 cm
• 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