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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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SmartVir — 1 UDI-DI variant, IVDD (SmartSeq s.r.l.)

MD Atlas
SmartSeq s.r.l.

Data from EUDAMED, last updated May 30, 2026

SmartVir

B-MF42241SVIRA7

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — General

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Manufacturer: SmartSeq s.r.l.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: B-MF42241SVIRA7
Device name: SmartVir
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Special device type: refdata.special-ivdd-device-type.software
Version date: Dec 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: SmartSeq s.r.l.
SRN: IT-MF-000042241
Country: Italy
Email: info@smartseq.it

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KC49R3E0917PAEHWMWF60AZV

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

SmartVirD-MF42241SVIRA7