gudid Primary ID: 1.0

Morphine300 Panel Dip (UDI 1.0)

Manufactured by ASSURE TECH. (HANGZHOU) CO., LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Morphine300 Panel Dip (Model/Catalog Number: 1.0) is a medical device manufactured by ASSURE TECH. (HANGZHOU) CO., LTD.. This product is indexed under FDA Product Code / Category Classification NGL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1.0
Product Code / EMDN: NGL
Device Name
Database Sync Date: 2026-08-09 09:05:25

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 Morphine300 Panel Dip?

The registered manufacturer of record for Morphine300 Panel Dip is ASSURE TECH. (HANGZHOU) CO., LTD..

What is the Primary UDI-DI identifier for Morphine300 Panel Dip?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.0.

What classification code is assigned to this device?

This device is registered under product classification code NGL.

Similar Classification Devices (NGL)

Other Devices by ASSURE TECH. (HANGZHOU) CO., LTD.

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