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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Get API Token Access ($49/mo)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.
Similar Classification Devices (G02060302)
Other Devices by THD S.P.A.
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