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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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Potilaan/vainajan suojaus, tuenta ja… — 8 UDI-DI variants, MDR

MD Atlas
Emicaid Oy

Data from EUDAMED, last updated May 23, 2026

Potilaan/vainajan suojaus, tuenta ja nosto

64199140088955VK

8 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: 64199140088955VK
Device name: Potilaan/vainajan suojaus, tuenta ja nosto
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 9, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01KC0TADFYCAQY2DY6SSE108QA

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

5600006419914002101
7814006419914002255
5710006419914002118
5201206419914002026
7854006419914002262
5387006419914002033
57401N06419914002125
52011S06419914002019