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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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StomFoam — 5 UDI-DI variants, MDR (ALP ecology s.r.o.)

MD Atlas
ALP ecology s.r.o.

Data from EUDAMED, last updated May 23, 2026

StomFoam

859403252F1VP

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: ALP ecology s.r.o.

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 859403252F1VP
Device name: StomFoam
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: ALP ecology s.r.o.
SRN: CZ-MF-000036962
Country: Czechia
Email: info@alpecology.cz
Phone: +420 596 636 107

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K09SF1SDD5E7Y3GN47DNTDB5

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

N/A08594032524204
N/A08594032520220
N/A08594032524228
N/A08594032524181
N/A08594032520244