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gudid Primary ID: 473572086

RIWO D-URS (UDI 473572086)

Manufactured by Richard Wolf GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RIWO D-URS - Primary ID 473572086

Device Regulatory Overview

The RIWO D-URS (Model/Catalog Number: 473572086) is a medical device manufactured by Richard Wolf GmbH. This product is indexed under FDA Product Code / Category Classification FGB within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

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Technical Specifications

Model Number
473572086
Product Code / EMDN
FGB
Device Name
SENSOR-URETERORENOSCOPE 9FR WL 600MM flexible, working channel 1: 3,6 Fr, working channel 2: 1,65 Fr, PACK = 3 pcs., can be used with vacuum aspiration and irrigation devices up to a maximum suction range of -450 mmHg/-60 kPa, sterile, for single use
Database Sync Date
2026-08-09 09:26:08

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 RIWO D-URS?

The registered manufacturer of record for RIWO D-URS is Richard Wolf GmbH.

What is the Primary UDI-DI identifier for RIWO D-URS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 473572086.

What classification code is assigned to this device?

This device is registered under product classification code FGB.

Similar Classification Devices (FGB)

Other Devices by Richard Wolf GmbH

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