eudamed_udi Primary ID: 00642790850153

ScarSil (UDI 00642790850153)

Manufactured by Scar Heal

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ScarSil (Model/Catalog Number: 85015) is a medical device manufactured by Scar Heal. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 85015
Product Code / EMDN: M04040701
Device Name: RejuvaSil Silicone Scar Gel
Database Sync Date: 2026-08-09 16:28:49

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 ScarSil?

The registered manufacturer of record for ScarSil is Scar Heal.

What is the Primary UDI-DI identifier for ScarSil?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00642790850153.

What classification code is assigned to this device?

This device is registered under product classification code M04040701.

Similar Classification Devices (M04040701)

Other Devices by Scar Heal

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