eudamed_udi Primary ID: D-3615370000375T2

LABORATOIRE MARQUE VERTE (UDI D-3615370000375T2)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The LABORATOIRE MARQUE VERTE (Model/Catalog Number: TH839S) is a medical device manufactured by Radiant Innovation Inc.. This product is indexed under FDA Product Code / Category Classification V0301010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TH839S
Product Code / EMDN: V0301010202
Device Name: TH839S
Database Sync Date: 2026-08-09 18:50:47

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 LABORATOIRE MARQUE VERTE?

The registered manufacturer of record for LABORATOIRE MARQUE VERTE is Radiant Innovation Inc..

What is the Primary UDI-DI identifier for LABORATOIRE MARQUE VERTE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-3615370000375T2.

What classification code is assigned to this device?

This device is registered under product classification code V0301010202.

Similar Classification Devices (V0301010202)

Other Devices by Radiant Innovation Inc.

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