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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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Gél anorektálny RECTOVENAL Acute s… — 4 UDI-DI variants, MDR

MD Atlas
VULM s.r.o.

Data from EUDAMED, last updated May 31, 2026

Gél anorektálny RECTOVENAL Acute s aplikátorom

8588010113RECTOVENALNF

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: VULM s.r.o.

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Device characteristics

Incorporates a medicinal product

Identity & classification

Basic UDI-DI: 8588010113RECTOVENALNF
Device name: Gél anorektálny RECTOVENAL Acute s aplikátorom
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: VULM s.r.o.
SRN: SK-MF-000001981
Country: Slovakia
Email: info@vulm.sk
Phone: +421917827470

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KRX427JAQHVHTM0A4B3AYMCH

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

ZV-1490034-0308588006802276
ZV-149002408588005606998
ZV-149002408588005606318
ZV-1490034-0308588006802283