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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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Seronorm® Cardiac Acute Lyo L-3 — 1 UDI-DI variant, IVDD (SERO AS)

MD Atlas
SERO AS

Data from EUDAMED, last updated May 30, 2026

Seronorm® Cardiac Acute Lyo L-3

B-17090041921846

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: SERO AS

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Device characteristics

Professional testingHuman tissues / cells

Identity & classification

Basic UDI-DI: B-17090041921846
Device name: Seronorm® Cardiac Acute Lyo L-3
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — General
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: SERO AS
SRN: NO-MF-000012954
Country: Norway
Email: sales@sero.no
Phone: +47 66858946

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQVZDRYZ9HC3V80JTRX9AYF3

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

21230517090041921846