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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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RTPCR016 — 2 UDI-DI variants, IVDR (Vircell, S.L)

MD Atlas
Vircell, S.L

Data from EUDAMED, last updated May 23, 2026

RTPCR016

843604032RTPCR01601W4

2 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Manufacturer: Vircell, S.L

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 843604032RTPCR01601W4
Device name: —
Device model: RTPCR016
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class C
Version date: Nov 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: Vircell, S.L
SRN: ES-MF-000004099
Country: Spain
Email: Vircell.eudamed@vircell.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JDM7GMCD4Q26337SD7JNZBC6

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

RTPCR016-LP08436610290463
RTPCR016-LPD08436040329436