gudid Primary ID: 83-7025

RETRACTOR SPINA PER BLUEPRINT (UDI 83-7025)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The RETRACTOR SPINA **PER BLUEPRINT** (Model/Catalog Number: 83-7025) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification GAD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 83-7025
Product Code / EMDN: GAD
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 RETRACTOR SPINA PER BLUEPRINT?

The registered manufacturer of record for RETRACTOR SPINA **PER BLUEPRINT** is W.H. Holden, Inc..

What is the Primary UDI-DI identifier for RETRACTOR SPINA PER BLUEPRINT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 83-7025.

What classification code is assigned to this device?

This device is registered under product classification code GAD.

Similar Classification Devices (GAD)

Other Devices by W.H. Holden, Inc.

Programmatic Export

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RETRACTOR SPINA **PER BLUEPRINT** (UDI 83-7025)