RejuvaSil (UDI 80010)

Manufactured by Scar Heal

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RejuvaSil (Model/Catalog Number: 80010) is a medical device manufactured by Scar Heal. This product is indexed under FDA Product Code / Category Classification MDA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 80010
Product Code / EMDN: MDA
Device Name: RejuvaSil Silicone Scar Gel 10 ml
Database Sync Date: 2026-08-09 09:36:28

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of RejuvaSil?

The registered manufacturer of record for RejuvaSil is Scar Heal.

What is the Primary UDI-DI identifier for RejuvaSil?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80010.

What classification code is assigned to this device?

This device is registered under product classification code MDA.

Similar Classification Devices (MDA)

Other Devices by Scar Heal

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