gudid Primary ID: 10-0906

RONGEUR KERRISON 200/4mm (UDI 10-0906)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RONGEUR KERRISON 200/4mm (Model/Catalog Number: 10-0906) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification EMH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10-0906
Product Code / EMDN: EMH
Device Name
Database Sync Date: 2026-08-09 09:03:32

Full Regulatory Attributes

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{
    "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 RONGEUR KERRISON 200/4mm?

The registered manufacturer of record for RONGEUR KERRISON 200/4mm is W.H. Holden, Inc..

What is the Primary UDI-DI identifier for RONGEUR KERRISON 200/4mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-0906.

What classification code is assigned to this device?

This device is registered under product classification code EMH.

Similar Classification Devices (EMH)

Other Devices by W.H. Holden, Inc.

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