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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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Yleisletku imulaitteeseen — 7 UDI-DI variants, MDR (Emicaid Oy)

MD Atlas
Emicaid Oy

Data from EUDAMED, last updated May 23, 2026

Yleisletku imulaitteeseen

64199140088950V9

7 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Emicaid Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 64199140088950V9
Device name: Yleisletku imulaitteeseen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 2025

Manufacturer & authorised representative

Manufacturer

Name: Emicaid Oy
SRN: FI-MF-000040418
Country: Finland
Email: marketing@emicaid.fi

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01KBYSKA1RPZBBZ3GMZFJ01FFW

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

000-5306419914001845
000-6206419914001890
000-6006419914001883
000-5506419914001869
000-5806419914001876
000-5206419914001838
000-5406419914001852