MEDLOT

GUDID 06974795050035

Henan Maidingkang Medical Technology Co., Ltd.

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• Primary Device ID: 06974795050035
• NIH Device Record Key: 30d9873a-140d-4a69-9e69-b77ed333b1a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MEDLOT
• Version Model Number: 4cm*4m
• 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	06974795050035 [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: 2024-01-31
• Device Publish Date: 2024-01-23

On-Brand Devices [MEDLOT]

• 06974795050042: 4cm*2m
• 06974795050035: 4cm*4m
• 06974795050028: 10*18cm
• 06974795050011: 4*15cm