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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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IVD Sample Collection Kit — 1 UDI-DI variant, IVDR (RDA Spot, UAB)

MD Atlas
RDA Spot, UAB

Data from EUDAMED, last updated May 30, 2026

IVD Sample Collection Kit

477905472RDA001EM

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: RDA Spot, UAB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 477905472RDA001EM
Device name: IVD Sample Collection Kit
Device model: RDA001
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Apr 1, 2026

Manufacturer & authorised representative

Manufacturer

Name: RDA Spot, UAB
SRN: LT-MF-000027300
Country: Lithuania
Email: info@rdaspot.com
Phone: +37060807777

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KN3YWM6WP934NS3KPXF50W6E

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

IVD Sample Collection Kit04779054720108