eudamed_udi Primary ID: 48058945150007

Evo Specific SPA (UDI 48058945150007)

Manufactured by ABD SRL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Evo Specific SPA (Model/Catalog Number: 1N3100 G1) is a medical device manufactured by ABD SRL. This product is indexed under FDA Product Code / Category Classification W01020205 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1N3100 G1
Product Code / EMDN: W01020205
Device Name: Allergy SPA Grasses - Allergia SPA Graminacee
Database Sync Date: 2026-08-09 16:28:50

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 Evo Specific SPA?

The registered manufacturer of record for Evo Specific SPA is ABD SRL.

What is the Primary UDI-DI identifier for Evo Specific SPA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 48058945150007.

What classification code is assigned to this device?

This device is registered under product classification code W01020205.

Similar Classification Devices (W01020205)

Other Devices by ABD SRL

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