gudid Primary ID: 3904-03NSP/Y

Hydrodissection Cannulae (UDI 3904-03NSP/Y)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hydrodissection Cannulae (Model/Catalog Number: 3904-03NSP/Y) is a medical device manufactured by STERIMEDIX LIMITED. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 3904-03NSP/Y
Product Code / EMDN: MED
Device Name: 27g Hydrodissector Chang
Database Sync Date: 2026-08-09 09:59:16

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 Hydrodissection Cannulae?

The registered manufacturer of record for Hydrodissection Cannulae is STERIMEDIX LIMITED.

What is the Primary UDI-DI identifier for Hydrodissection Cannulae?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3904-03NSP/Y.

What classification code is assigned to this device?

This device is registered under product classification code MED.

Similar Classification Devices (MED)

Other Devices by STERIMEDIX LIMITED

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