GUDIDData
gudid Primary ID: ASUS-86-900R-DC

Ascend Single-Use Flexible Ureteroscope (UDI ASUS-86-900R-DC)

Manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ascend Single-Use Flexible Ureteroscope - Primary ID ASUS-86-900R-DC

Device Regulatory Overview

The Ascend Single-Use Flexible Ureteroscope (Model/Catalog Number: ASUS-86-900R-DC) is a medical device manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FGB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ASUS-86-900R-DC
Product Code / EMDN
FGB
Device Name
Database Sync Date
2026-08-09 09:06:41

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 Ascend Single-Use Flexible Ureteroscope?

The registered manufacturer of record for Ascend Single-Use Flexible Ureteroscope is Guangzhou Red Pine Medical Instrument Co., Ltd..

What is the Primary UDI-DI identifier for Ascend Single-Use Flexible Ureteroscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ASUS-86-900R-DC.

What classification code is assigned to this device?

This device is registered under product classification code FGB.

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