eudamed_udi Primary ID: 09555076111842

Nuzone X2 (UDI 09555076111842)

Manufactured by TERANG NUSA (MALAYSIA) SDN. BHD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Nuzone X2 (Model/Catalog Number: NX2-507611184) is a medical device manufactured by TERANG NUSA (MALAYSIA) SDN. BHD.. This product is indexed under FDA Product Code / Category Classification T01010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NX2-507611184
Product Code / EMDN: T01010201
Device Name: Sterile Polychloroprene Surgical Powder Free Gloves
Database Sync Date: 2026-08-09 16:28:53

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 Nuzone X2?

The registered manufacturer of record for Nuzone X2 is TERANG NUSA (MALAYSIA) SDN. BHD..

What is the Primary UDI-DI identifier for Nuzone X2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09555076111842.

What classification code is assigned to this device?

This device is registered under product classification code T01010201.

Similar Classification Devices (T01010201)

Other Devices by TERANG NUSA (MALAYSIA) SDN. BHD.

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