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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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VATA HIDROFILA DE UZ MEDICINAL — 15 UDI-DI variants, MDR

MD Atlas
EUROCOSMETIC s.r.l.

Data from EUDAMED, last updated May 31, 2026

VATA HIDROFILA DE UZ MEDICINAL

594074146VHMEDK4

15 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: EUROCOSMETIC s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 594074146VHMEDK4
Device name: VATA HIDROFILA DE UZ MEDICINAL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: EUROCOSMETIC s.r.l.
SRN: RO-MF-000000906
Country: Romania
Email: attila@izis.ro
Phone: +40723164556

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JTN3GZWS099KD4AABM3S8A7Q

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

IZIS100100K05940741460341
IZIS100200K05940741460273
IZIS100500K05940741460228
IZIS100500P05940741460235
IZIS100500V05940741460266
IZIS100200S05940741460310
IZIS100500S05940741460259
IZIS100100SZ05940741460327
IZIS100200SZ05940741460303
IZIS100500SZ05940741460334
IZIS100100P05940741460297
V100GIZIS05940741460280
V200GIZIS05940741460006
IZIS100200P05940741460365
VM200GIZ05940741460242