GUDIDData
gudid Primary ID: UV-US110-H(REV)

Flexible Video-Choledo-Cysto-Ureteroscope (UDI UV-US110-H(REV))

Manufactured by Shanghai SeeGen Photoelectric Technology Co.,Ltd. (YinDu Road Factory)

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flexible Video-Choledo-Cysto-Ureteroscope - Primary ID UV-US110-H(REV)

Device Regulatory Overview

The Flexible Video-Choledo-Cysto-Ureteroscope (Model/Catalog Number: UV-US110-H(REV)) is a medical device manufactured by Shanghai SeeGen Photoelectric Technology Co.,Ltd. (YinDu Road Factory). This product is indexed under FDA Product Code / Category Classification FGB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
UV-US110-H(REV)
Product Code / EMDN
FGB
Device Name
Database Sync Date
2026-08-09 09:06:39

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 Flexible Video-Choledo-Cysto-Ureteroscope?

The registered manufacturer of record for Flexible Video-Choledo-Cysto-Ureteroscope is Shanghai SeeGen Photoelectric Technology Co.,Ltd. (YinDu Road Factory).

What is the Primary UDI-DI identifier for Flexible Video-Choledo-Cysto-Ureteroscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UV-US110-H(REV).

What classification code is assigned to this device?

This device is registered under product classification code FGB.

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