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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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Vakuová dlaha krku — 39 UDI-DI variants, MDR (VAKUFORM s.r.o.)

MD Atlas
VAKUFORM s.r.o.

Data from EUDAMED, last updated May 23, 2026

Vakuová dlaha krku

859422551VAKUFORMHR

39 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: VAKUFORM s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859422551VAKUFORMHR
Device name: Vakuová dlaha krku
Device model: VAKUOVÉ DLAHY A MATRACE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: VAKUFORM s.r.o.
SRN: CZ-MF-000044602
Country: Czechia
Email: vakuform@vakuform.cz
Phone: +420577211676

Variants by status

UDI-DI variants

39 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQVEQ5METYY48VVCFD4T7E5H

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

VM-189/108594225510649
VM-180/108594225510625
VM-184/1 08594225510656
VM-185/1 08594225510663
VM-178/208594225510748
VS-20508594225510182
VS-20408594225510175
VS-20908594225510205
VS-20808594225510199
VS-20308594225510090
VS-20208594225510083
VS-202/208594225510212
VS-203/208594225510106
VM-203/208594225510533

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