MEDLOT

GUDID 06974795050103

Henan Maidingkang Medical Technology Co., Ltd.

Scar-management dressing, reusable

• Primary Device ID: 06974795050103
• NIH Device Record Key: 2ead236f-19c0-4a4c-80c4-eb3a3fc0a267
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDLOT
• Version Model Number: 4cm*2m
• Company DUNS: 724981491
• Company Name: Henan Maidingkang Medical Technology Co., Ltd.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	06974795050103 [Primary]

FDA Product Code

• PFP: Silicone Hydrogel For Scar Management

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: 2024-07-10
• Device Publish Date: 2024-07-02

On-Brand Devices [MEDLOT]

• 06974795050042: 4cm*2m
• 06974795050035: 4cm*4m
• 06974795050028: 10*18cm
• 06974795050011: 4*15cm
• 06974795057157: 4*15cm
• 06974795050103: 4cm*2m
• 06974795056358: 4cm*2m
• 06974795053364: 4cm*2m
• 06974795051872: 4*15cm
• 06974795058772: 4*15cm
• 06974795052824: 10*18cm