GUDIDData
eudamed_udi Primary ID: 06438408004490

Inion FreedomPin Instrumentation (UDI 06438408004490)

Manufactured by Inion Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Inion FreedomPin Instrumentation - Primary ID 06438408004490

Device Regulatory Overview

The Inion FreedomPin Instrumentation (Model/Catalog Number: INS-9283) is a medical device manufactured by Inion Oy. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
INS-9283
Product Code / EMDN
L091001
Device Name
Inion Instruments
Database Sync Date
2026-08-09 16:29:05

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 Inion FreedomPin Instrumentation?

The registered manufacturer of record for Inion FreedomPin Instrumentation is Inion Oy.

What is the Primary UDI-DI identifier for Inion FreedomPin Instrumentation?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438408004490.

What classification code is assigned to this device?

This device is registered under product classification code L091001.

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