gudid Primary ID: TROLLI T30 MIS.43

TROLLI (UDI TROLLI T30 MIS.43)

Manufactured by ORMESA SRL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The TROLLI (Model/Catalog Number: TROLLI T30 MIS.43) is a medical device manufactured by ORMESA SRL. This product is indexed under FDA Product Code / Category Classification INM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TROLLI T30 MIS.43
Product Code / EMDN: INM
Device Name: TROLLI is a wheelchair designed to facilitate the displacement of adults and children with walking issues: subjects with pathological pictures that do not requirespecific postural measures and that do not have complete autonomy. It allows the positioning of the user with disabilities of varying complexity, in the most appropriate and functional posture in the different everyday environments. The postural components (supports and belts) allow to give stability to the pelvis, lower limbs and trunk. It can be used even in medium severity circumstances, in outdoor and indoor environments, for the transport of those subjects, who are not able to independently maintain the seating posture due to severe disorders of the nervous and muscle system or of the rational sphere.
Database Sync Date: 2026-08-09 09:04:30

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 TROLLI?

The registered manufacturer of record for TROLLI is ORMESA SRL.

What is the Primary UDI-DI identifier for TROLLI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TROLLI T30 MIS.43.

What classification code is assigned to this device?

This device is registered under product classification code INM.

Similar Classification Devices (INM)

Other Devices by ORMESA SRL

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