GUDIDData
eudamed_udi Primary ID: 08904148100085

ACE Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope (UDI 08904148100085)

Manufactured by ACE MEDICAL DEVICES PVT LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACE Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope - Primary ID 08904148100085

Device Regulatory Overview

The ACE Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope (Model/Catalog Number: BS-DC-24F-0) is a medical device manufactured by ACE MEDICAL DEVICES PVT LTD. This product is indexed under FDA Product Code / Category Classification K0201010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BS-DC-24F-0
Product Code / EMDN
K0201010301
Device Name
TURP Loop/ Electrode- Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope
Database Sync Date
2026-08-09 16:29:50

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 ACE Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope?

The registered manufacturer of record for ACE Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope is ACE MEDICAL DEVICES PVT LTD.

What is the Primary UDI-DI identifier for ACE Bipolar Cutting Loop Electrode, 24 Fr, 0°, Double Stem, Compatible with Storz Brand Resectoscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08904148100085.

What classification code is assigned to this device?

This device is registered under product classification code K0201010301.

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