NA (UDI PI-3415)

Manufactured by PACIFIC INSTRUMENTS, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: PI-3415) is a medical device manufactured by PACIFIC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HTW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PI-3415
Product Code / EMDN: HTW
Device Name: 3.5mm Drill Bit, AO QC
Database Sync Date: 2026-08-09 09:12:18

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 NA?

The registered manufacturer of record for NA is PACIFIC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PI-3415.

What classification code is assigned to this device?

This device is registered under product classification code HTW.

Similar Classification Devices (HTW)

Other Devices by PACIFIC INSTRUMENTS, INC.

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