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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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!M1 — 1 UDI-DI variant, MDD (Solutions for tomorrow AB)

MD Atlas
Solutions for tomorrow AB

Data from EUDAMED, last updated May 30, 2026

!M1

B-07350011170012

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: Solutions for tomorrow AB

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Device characteristics

Active device

Legacy certificates

Certificate number: 1434-MDD-386/2021
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: Apr 7, 2024

Identity & classification

Basic UDI-DI: B-07350011170012
Device name: !M1
Device model: !M1
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Oct 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Solutions for tomorrow AB
SRN: SE-MF-000027431
Country: Sweden
Email: info@solutionsfortomorrow.se
Phone: 0104564500

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GF0JPMD7GYBCEQQB0M9G6QY5

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

!M107350011170012