gudid Primary ID: UP18250-00

UNIVERSAL PLUS (UDI UP18250-00)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The UNIVERSAL PLUS (Model/Catalog Number: UP18250-00) is a medical device manufactured by MEDAX SRL UNIPERSONALE. This product is indexed under FDA Product Code / Category Classification KNW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: UP18250-00
Product Code / EMDN: KNW
Device Name: Biopsy needle 18G x 250 mm
Database Sync Date: 2026-08-09 09:04:29

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 UNIVERSAL PLUS?

The registered manufacturer of record for UNIVERSAL PLUS is MEDAX SRL UNIPERSONALE.

What is the Primary UDI-DI identifier for UNIVERSAL PLUS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UP18250-00.

What classification code is assigned to this device?

This device is registered under product classification code KNW.

Similar Classification Devices (KNW)

Other Devices by MEDAX SRL UNIPERSONALE

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