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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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SIRINGA PRERIEMPITA — 4 UDI-DI variants, MDR (PENTAFERTE ITALIA SRL)

MD Atlas
PENTAFERTE ITALIA SRL

Data from EUDAMED, last updated May 31, 2026

SIRINGA PRERIEMPITA

801526210854

4 UDI-DI variants

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

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

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 801526210854
Device name: SIRINGA PRERIEMPITA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: PENTAFERTE ITALIA SRL
SRN: IT-MF-000040982
Country: Italy
Email: rosa.digioia@numantec.eu
Phone: +39 0861 560201

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KEEDSKTG6TQ51CH9WN6ZD3MR

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

SIRINGA PRERIEMPITA 10 ML 0,9% NaCl- PENTAFLUSH08015262000219
SIRINGA PRERIEMPITA 20 ML 0,9% NaCl- PENTAFLUSH08015262000226
SIRINGA PRERIEMPITA 3 ML 0,9% NaCl- PENTAFLUSH08015262000196
SIRINGA PRERIEMPITA 5 ML 0,9% NaCl- PENTAFLUSH08015262000202