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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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MONOCLEAN TYPE 20 — 2 UDI-DI variants, MDR (PHARMA EEC SRL)

MD Atlas
PHARMA EEC SRL

Data from EUDAMED, last updated May 30, 2026

MONOCLEAN TYPE 20

805625479IMMOBGS

2 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: PHARMA EEC SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805625479IMMOBGS
Device name: MONOCLEAN TYPE 20
Device model: MONO 20
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: PHARMA EEC SRL
SRN: IT-MF-000037561
Country: Italy
Email: pharma@pharma.it
Phone: +390521788222

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HK7Q5JET2HTEREN314D4BTPP

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

MONOCLEAN TYPE 2008056254790015
MONO 20 C/A08056254790022