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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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UNISTERI HP; UNISTERI SL — 2 UDI-DI variants, MDR

MD Atlas
BMT Medical Technology s.r.o.

Data from EUDAMED, last updated May 23, 2026

UNISTERI HP; UNISTERI SL

859420341SPSRT

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BMT Medical Technology s.r.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 859420341SPSRT
Device name: UNISTERI HP; UNISTERI SL
Device model: SPS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 8, 2022

Manufacturer & authorised representative

Manufacturer

Name: BMT Medical Technology s.r.o.
SRN: CZ-MF-000001680
Country: Czechia
Email: regulatory@bmt.cz

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G7S19M2FBPTEP34N0VHAHCHA

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

SPS08594203410046
SPS08594203410510