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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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SafeR Syringe — 5 UDI-DI variants, MDR (Roncadelle Operations Srl)

MD Atlas
Roncadelle Operations Srl

Data from EUDAMED, last updated May 30, 2026

SafeR Syringe

805699902SyringeCP00201F9

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: Roncadelle Operations Srl

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 805699902SyringeCP00201F9
Device name: SafeR Syringe
Device model: SFS0100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: Roncadelle Operations Srl
SRN: IT-MF-000017979
Country: Italy
Email: info@roncadelle-operations.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G9PJ22ZFHVSK1CSQ0BFT5FGG

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

SFS022508056999020026
SFS050008056999020040
SFS030008056999020033
SFS010008056999020002
SFS020008056999020019