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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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Patient monitor UM 300-10-S — 1 UDI-DI variant, MDD

MD Atlas
UTAS Technologies

Data from EUDAMED, last updated May 30, 2026

Patient monitor UM 300-10-S

B-8588009324508AY

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: UTAS Technologies

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Device characteristics

Active device

Legacy certificates

Certificate number: 144878-19-04-04
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: CE Certiso Orvos- és Kórháztechnikai Ellenőrző és Tanúsító Kft. (2409)
Validity: Apr 3, 2024

Identity & classification

Basic UDI-DI: B-8588009324508AY
Device name: Patient monitor UM 300-10-S
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: UTAS Technologies
SRN: SK-MF-000022644
Country: Slovakia
Email: info@utastech.eu
Phone: +421220620001

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HKFYY9EMJ8WMC2VA050HS9XT

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

UM 300-10-SD-8588009324508AY