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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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Varpaanerottaja — 36 UDI-DI variants, MDR

MD Atlas
Suomen Hoitolatukku Tuonti Oy

Data from EUDAMED, last updated May 23, 2026

Varpaanerottaja

6416078TOESEP4C

36 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: Suomen Hoitolatukku Tuonti Oy

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 6416078TOESEP4C
Device name: Varpaanerottaja
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Suomen Hoitolatukku Tuonti Oy
SRN: FI-MF-000011716
Country: Finland
Email: info@hoitolatukku.fi
Phone: +35822122200

Variants by status

UDI-DI variants

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FS1QA1PTF9A5Z4DM3YRN05VH

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

92001039C06416078010393
92001038C06416078010386
92001037C06416078010379
92003030M06416078030308
92003028M06416078030285
92003026M06416078030261
920030372CL06416078037215
920030374CR06416078037420
920030372CR06416078037222
920030374CL06416078037413
920030202206416078020217

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