gudid Primary ID: 525-506

ARMSTRONG VENT TUBE (UDI 525-506)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ARMSTRONG VENT TUBE (Model/Catalog Number: 525-506) is a medical device manufactured by Grace Medical, Inc.. This product is indexed under FDA Product Code / Category Classification ETD within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2308-2026 View Full Alert →

TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis...

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Technical Specifications

Model Number: 525-506
Product Code / EMDN: ETD
Device Name: ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 60 PACK
Database Sync Date: 2026-08-09 09:59:39

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 ARMSTRONG VENT TUBE?

The registered manufacturer of record for ARMSTRONG VENT TUBE is Grace Medical, Inc..

What is the Primary UDI-DI identifier for ARMSTRONG VENT TUBE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 525-506.

What classification code is assigned to this device?

This device is registered under product classification code ETD.

Similar Classification Devices (ETD)

Other Devices by Grace Medical, Inc.

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