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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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Stethoscope Tube — 10 UDI-DI variants, MDR (1M4 OÜ)

MD Atlas
1M4 OÜ

Data from EUDAMED, last updated May 23, 2026

Stethoscope Tube

474501056412000BE

10 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: 1M4 OÜ

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 474501056412000BE
Device name: Stethoscope Tube
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: 1M4 OÜ
SRN: EE-MF-000040367
Country: Estonia
Email: info@1m4.eu

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01JNN7V926VTGB7V0X6DXPBPTE

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

12000.0804745010564703
12000.0904745010564710
12000.0404745010564666
12000.0304745010564659
12000.0704745010564697
12000.1004745010564727
12000.0604745010564680
12000.0104745010564635
12000.0204745010564642
12000.0504745010564673