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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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Seramun SpotSight plate mono — 2 UDI-DI variants, IVDR

MD Atlas
Seramun Diagnostica GmbH

Data from EUDAMED, last updated May 23, 2026

Seramun SpotSight plate mono

4099466SPPLATEEZ

2 UDI-DI variants

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: Seramun Diagnostica GmbH

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 4099466SPPLATEEZ
Device name: Seramun SpotSight plate mono
Device model: Seramun SpotSight plate mono
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Seramun Diagnostica GmbH
SRN: DE-MF-000026029
Country: Germany
Email: info@seramun.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPN3VF5YM3SQ0HHMGP6ENDG1

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

SP-PLATE-C04099466360113
SP-PLATE-D04099466360212