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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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FisioEnema — 2 UDI-DI variants, MDR (Casen Recordati, S.L.)

MD Atlas
Casen Recordati, S.L.

Data from EUDAMED, last updated May 23, 2026

FisioEnema

8437013001FISIOENEMAXC

2 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: Casen Recordati, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437013001FISIOENEMAXC
Device name: FisioEnema
Device model: FisioEnema 250 ml
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 19, 2023

Manufacturer & authorised representative

Manufacturer

Name: Casen Recordati, S.L.
SRN: ES-MF-000002442
Country: Spain
Email: info@casenrecordati.com
Phone: +34 91 351 88 00

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01H0SJTBM0ZN1A8JYXXJ1C4SQF

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

202574.508437013001335
240303.108437013001342