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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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Emergenza — 6 UDI-DI variants, MDR (RAM Apparecchi Medicali srl)

MD Atlas
RAM Apparecchi Medicali srl

Data from EUDAMED, last updated May 30, 2026

Emergenza

805188221EMERGENZADZ

6 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: RAM Apparecchi Medicali srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805188221EMERGENZADZ
Device name: Emergenza
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: RAM Apparecchi Medicali srl
SRN: IT-MF-000015826
Country: Italy
Email: ram@elettromedicali.it
Phone: +390105761476

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FW1MG5DJ7PSZ5CDTF89WYSPX

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

PS0RATS00108051882210508
PS0RABP00308051882210485
PS0RASP0208051882210522
PS0RABP00108051882210478
PS0RASP0108051882210515
PS0RAZ0108051882210492