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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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Ortoottinen pohjallinen, elementti,… — 7 UDI-DI variants, MDR

MD Atlas
Suomen Hoitolatukku Tuonti Oy

Data from EUDAMED, last updated May 23, 2026

Ortoottinen pohjallinen, elementti, ei-antimikrobinen

6416078ORTHINS9P

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: Suomen Hoitolatukku Tuonti Oy

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 6416078ORTHINS9P
Device name: Ortoottinen pohjallinen, elementti, ei-antimikrobinen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 24, 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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GB7D84B7DZATMGNSSF6ABC0R

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

92005040L06416078050405
92005040S06416078005047
92005127SC06416078051273
92005126SC06416078051266
9200811106416078081119
9200608M06416078006082
92005125SC06416078051259