Mepilex® Border Post-Op Ag

GUDID 07333350561192

Mepilex Border Post-Op Ag 9x10cm

Mölnlycke Health Care AB

Wound-nonadherent dressing, absorbent, antimicrobial

• Primary Device ID: 07333350561192
• NIH Device Record Key: 43ef7ccf-bc5a-43bb-b366-f4c7f74363be
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepilex® Border Post-Op Ag
• Version Model Number: 498200
• Company DUNS: 631770658
• Company Name: Mölnlycke Health Care AB
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	07333350518240 [Primary]
GS1	07333350561192 [Package]; Contains: 07333350883300; Package: CASE [10 Units]; In Commercial Distribution
GS1	07333350883300 [Package]; Contains: 07333350518240; Package: PACK_OR_INNER_PACK [5 Units]; In Commercial Distribution

FDA Product Code

• FRO: Dressing, wound, drug

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: 2023-06-27
• Device Publish Date: 2023-06-19

On-Brand Devices [Mepilex® Border Post-Op Ag]

• 07323190142583: Mepilex Border Post-Op Ag 10x35cm
• 07323190142545: Mepilex Border Post-Op Ag 10x30cm
• 07323190142507: Mepilex Border Post-Op Ag 10x25cm
• 07323190142460: Mepilex Border Post-Op Ag 10x20cm
• 07323190142422: Mepilex Border Post-Op Ag 10x15cm
• 07333350513627: Mepilex Border Post-Op Ag 10x25cm
• 07333350902957: Mepilex Border Post-Op Ag 10x35cm
• 07333350246792: Mepilex Border Post-Op Ag 6x8cm
• 07333350085933: Mepilex Border Post-Op Ag 10x20cm
• 07333350561192: Mepilex Border Post-Op Ag 9x10cm
• 07333350450526: Mepilex Border Post-Op Ag 10x15cm
• 07333350958978: Mepilex Border Post-Op Ag 10x30cm