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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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BULION SELENIT trusa (800+200) — 1 UDI-DI variant, IVDR

MD Atlas
SC MEDICAMED MARKET SRL

Data from EUDAMED, last updated May 30, 2026

BULION SELENIT trusa (800+200)

594065202M1535610003Q

1 UDI-DI variant

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: SC MEDICAMED MARKET SRL

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 594065202M1535610003Q
Device name: BULION SELENIT trusa (800+200)
Device model: BULION SELENIT trusa (800+200)
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 4, 2025

Manufacturer & authorised representative

Manufacturer

Name: SC MEDICAMED MARKET SRL
SRN: RO-MF-000002243
Country: Romania
Email: office@medicamed.ro
Phone: +40742156700

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JK892D9J8HPDMNRNM30MKHWN

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

M15356100005940652024526