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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CARROZZINE — 5 UDI-DI variants, MDR (INTERMED SRL)

MD Atlas
INTERMED SRL

Data from EUDAMED, last updated May 30, 2026

CARROZZINE

805267997CARROZZINE25

5 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: INTERMED SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805267997CARROZZINE25
Device name: —
Device model: CARROZZINE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: INTERMED SRL
SRN: IT-MF-000013039
Country: Italy
Email: augusto.gussoni@intermeditalia.it

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G8K6AKZBS19YB1651SV59C6T

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

E-LIGHT2-37T08052679970032
NAR-A0108052679979165
NARROW-4008052679970001
NARROW-4508052679970025
NARROW-4308052679970018