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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 — 6 UDI-DI variants, MDR (SC SPD STAR SRL)

MD Atlas
SC SPD STAR SRL

Data from EUDAMED, last updated May 30, 2026

VATA HIDROFILA

5944751VATAAJ

6 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: SC SPD STAR SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5944751VATAAJ
Device name: VATA HIDROFILA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 16, 2022

Manufacturer & authorised representative

Manufacturer

Name: SC SPD STAR SRL
SRN: RO-MF-000004404
Country: Romania
Email: OFFICE@SPDGROUP.RO
Phone: 0040264223495

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01G36J5Y50QQPECZD7SWVZFYM9

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

VC10005944751000528
VC20005944751000429
VO10005944751000320
VO20005944751000511
VN20005944751000412
VN10005944751000658