GUDIDData
eudamed_udi Primary ID: 08033737710463

THD LIGHT-SCOPE MINI-RECTO (LED INS/NS) (UDI 08033737710463)

Manufactured by THD S.P.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for THD LIGHT-SCOPE MINI-RECTO (LED INS/NS) - Primary ID 08033737710463

Device Regulatory Overview

The THD LIGHT-SCOPE MINI-RECTO (LED INS/NS) (Model/Catalog Number: 800100) is a medical device manufactured by THD S.P.A.. This product is indexed under FDA Product Code / Category Classification G02060302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
800100
Product Code / EMDN
G02060302
Device Name
THD Not Sterile AnoProctoRectoscopes LED and not LED
Database Sync Date
2026-08-09 16:28:45

Full Regulatory Attributes

🔒 Token Gated
{
    "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 THD LIGHT-SCOPE MINI-RECTO (LED INS/NS)?

The registered manufacturer of record for THD LIGHT-SCOPE MINI-RECTO (LED INS/NS) is THD S.P.A..

What is the Primary UDI-DI identifier for THD LIGHT-SCOPE MINI-RECTO (LED INS/NS)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033737710463.

What classification code is assigned to this device?

This device is registered under product classification code G02060302.

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