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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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Polohovací pomůcky Sláva — 36 UDI-DI variants, MDR

MD Atlas
SORAL medical s.r.o.

Data from EUDAMED, last updated May 31, 2026

Polohovací pomůcky Sláva

859421180PP01GY

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: SORAL medical s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859421180PP01GY
Device name: Polohovací pomůcky Sláva
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: SORAL medical s.r.o.
SRN: CZ-MF-000030397
Country: Czechia
Email: info@soral.eu
Phone: +420 251 611 915

Variants by status

UDI-DI variants

36 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSN7S2EK3CDV1Q9MR2SPD4PY

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

210-S28-V08594211800334
210-S29-V08594211800341
210-S3-V08594211800044
210-S4-V08594211800051
210-S5-V08594211800068
210-S6-V08594211800075
210-S7-V08594211800082
210-S8-V08594211800099
210-S9-V08594211800105
210-Snek-V08594211800358
210-VK-V08594211800402

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