GUDID 16974795050131

Scar Sticker (Sterile)

Henan Maidingkang Medical Technology Co., Ltd.

Scar management dressing, single-use, sterile

• Primary Device ID: 16974795050131
• NIH Device Record Key: d800cfc8-0079-47ab-90e1-3ce711696b01
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: Sterile
• 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: true
• 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	06974795050134 [Primary]
GS1	16974795050131 [Package]; Contains: 06974795050134; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• PFP: Silicone Hydrogel For Scar Management

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: 2022-06-13
• Device Publish Date: 2022-06-03

Devices Manufactured by Henan Maidingkang Medical Technology Co., Ltd.

• 06974795051810 - MDK-MEDICAL: 2025-05-01
• 06974795051896 - MDK-MEDICAL: 2025-05-01
• 06974795053777 - MDK-MEDICAL: 2025-05-01
• 06974795054101 - MDK-MEDICAL: 2025-05-01
• 06974795054736 - MDK-MEDICAL: 2025-05-01
• 06974795055504 - MDK-MEDICAL: 2025-05-01
• 06974795055948 - MDK-MEDICAL: 2025-05-01
• 06974795056174 - MDK-MEDICAL: 2025-05-01