gudid Primary ID: HY-525

HYGITECH (UDI HY-525)

Manufactured by HYGITECH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HYGITECH (Model/Catalog Number: HY-525) is a medical device manufactured by HYGITECH. This product is indexed under FDA Product Code / Category Classification FXP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HY-525
Product Code / EMDN: FXP
Device Name: Standard waterproof absorbent surgical drape.Sterile dual layered surgical drape, absorbent and impermeable, ensures the best protection!Protects the equipment, tables and the patient's chest and shoulders.
Database Sync Date: 2026-08-09 09:26:35

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 HYGITECH?

The registered manufacturer of record for HYGITECH is HYGITECH.

What is the Primary UDI-DI identifier for HYGITECH?

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

What classification code is assigned to this device?

This device is registered under product classification code FXP.

Similar Classification Devices (FXP)

Other Devices by HYGITECH

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