eudamed_udi Primary ID: D-FT.CE.114.FB.678

SOFIMAR HA (UDI D-FT.CE.114.FB.678)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SOFIMAR HA (Model/Catalog Number: FT.CE.114.FB.6) is a medical device manufactured by GRUPPO FARMAIMPRESA SRL. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FT.CE.114.FB.6
Product Code / EMDN: Q030199
Device Name: SOFIMAR HA
Database Sync Date: 2026-08-09 16:30:25

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 SOFIMAR HA?

The registered manufacturer of record for SOFIMAR HA is GRUPPO FARMAIMPRESA SRL.

What is the Primary UDI-DI identifier for SOFIMAR HA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-FT.CE.114.FB.678.

What classification code is assigned to this device?

This device is registered under product classification code Q030199.

Similar Classification Devices (Q030199)

Other Devices by GRUPPO FARMAIMPRESA SRL

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