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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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Vaivaisenluunsuoja — 12 UDI-DI variants, MDR

MD Atlas
Suomen Hoitolatukku Tuonti Oy

Data from EUDAMED, last updated May 23, 2026

Vaivaisenluunsuoja

6416078HALVALTX

12 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6416078HALVALTX
Device name: Vaivaisenluunsuoja
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 16, 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

12 UDI-DI variants

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Applied filters

basicUdiUlid01FSHNVD8XWE8GCKZWKFCX083S

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

9200130106416078013011
9200130006416078013004
92001319M06416078013196
92001305206416078130527
92001305406416078130541
92001305306416078130534
92001305106416078130510
92001304MC06416078013042
92001303MC06416078013035
9200131506416078013158
9200131706416078013172
9200821206416078082123