Mepilex® Border Post-Op

GUDID 07323190183241

Mepilex Border Post-Op 4x8in/10x20cm, CVS

Mölnlycke Health Care AB

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• Primary Device ID: 07323190183241
• NIH Device Record Key: 30a10541-4f5b-4a6d-a7c4-fee8856fe61e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mepilex® Border Post-Op
• Version Model Number: 495388
• 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

Device Dimensions

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Device Identifiers

Device Issuing Agency	Device ID
GS1	07323190183241 [Package]; Contains: 07323190183258; Package: [14 Units]; Discontinued: 1995-12-31; Not in Commercial Distribution
GS1	07323190183258 [Package]; Contains: 07323190183371; Package: [2 Units]; Discontinued: 1995-12-31; Not in Commercial Distribution
GS1	07323190183371 [Primary]

FDA Product Code

• NAC: Dressing, wound, hydrophilic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-05
• Device Publish Date: 2020-07-28

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

• 07323190183241: Mepilex Border Post-Op 4x8in/10x20cm, CVS
• 07323190282746: Mepilex Border Post Op 10x35cm
• 07323190236961: Mepilex Border Post Op 10x25cm
• 07323190236886: Mepilex Border Post Op 10x20cm
• 07323190236800: Mepilex Border Post Op 10x15cm
• 07323190237043: Mepilex Border Post Op 10x30cm
• 07323190236756: Mepilex Border Post Op 9x10cm
• 07323190236718: Mepilex Border Post Op 6x8cm