POSKOM Co., Ltd. (UDI PXP-20HF)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The POSKOM Co., Ltd. (Model/Catalog Number: PXP-20HF) is a medical device manufactured by Poskom Co., Ltd.. This product is indexed under FDA Product Code / Category Classification IZL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PXP-20HF
Product Code / EMDN: IZL
Device Name
Database Sync Date: 2026-08-09 09:18:55

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 POSKOM Co., Ltd.?

The registered manufacturer of record for POSKOM Co., Ltd. is Poskom Co., Ltd..

What is the Primary UDI-DI identifier for POSKOM Co., Ltd.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PXP-20HF.

What classification code is assigned to this device?

This device is registered under product classification code IZL.

Similar Classification Devices (IZL)

Other Devices by Poskom Co., Ltd.

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