gudid Primary ID: 91-0121

LEVEL ONE, REDUCTION, BONE, STERNAL MODIFIED (UDI 91-0121)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The LEVEL ONE, REDUCTION, BONE, STERNAL MODIFIED (Model/Catalog Number: 91-0121) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification HTD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 91-0121
Product Code / EMDN: HTD
Device Name
Database Sync Date: 2026-08-09 09:01:13

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 LEVEL ONE, REDUCTION, BONE, STERNAL MODIFIED?

The registered manufacturer of record for LEVEL ONE, REDUCTION, BONE, STERNAL MODIFIED is W.H. Holden, Inc..

What is the Primary UDI-DI identifier for LEVEL ONE, REDUCTION, BONE, STERNAL MODIFIED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 91-0121.

What classification code is assigned to this device?

This device is registered under product classification code HTD.

Similar Classification Devices (HTD)

Other Devices by W.H. Holden, Inc.

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