gudid Primary ID: 83-2000-3

BRACKET HOLDING INST CVD MODIF (UDI 83-2000-3)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BRACKET HOLDING INST CVD MODIF (Model/Catalog Number: 83-2000-3) 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: 83-2000-3
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 BRACKET HOLDING INST CVD MODIF?

The registered manufacturer of record for BRACKET HOLDING INST CVD MODIF is W.H. Holden, Inc..

What is the Primary UDI-DI identifier for BRACKET HOLDING INST CVD MODIF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 83-2000-3.

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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