gudid Primary ID: 903T-DL-100

Premium Plus (UDI 903T-DL-100)

Manufactured by Premium Plus (Dongguan) Limited

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Premium Plus (Model/Catalog Number: 903T-DL-100) is a medical device manufactured by Premium Plus (Dongguan) Limited. This product is indexed under FDA Product Code / Category Classification KXR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 903T-DL-100
Product Code / EMDN: KXR
Device Name: Micro Applicators
Database Sync Date: 2026-08-09 09:01:55

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 Premium Plus?

The registered manufacturer of record for Premium Plus is Premium Plus (Dongguan) Limited.

What is the Primary UDI-DI identifier for Premium Plus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 903T-DL-100.

What classification code is assigned to this device?

This device is registered under product classification code KXR.

Similar Classification Devices (KXR)

Other Devices by Premium Plus (Dongguan) Limited

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