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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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Hydrogél Berovenal — 1 UDI-DI variant, MDR (VULM s.r.o.)

MD Atlas
VULM s.r.o.

Data from EUDAMED, last updated May 31, 2026

Hydrogél Berovenal

8588006802Berovenal2Q

1 UDI-DI variant

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

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

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 8588006802Berovenal2Q
Device name: Hydrogél Berovenal
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 27, 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

1 UDI-DI variant

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basicUdiUlid01KSME5XS968YCM3SZ4CKXZ90D

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-1670024-0108588006802122