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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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Let's Dream — 3 UDI-DI variants, MDR (Trust Care AB)

MD Atlas
Trust Care AB

Data from EUDAMED, last updated May 30, 2026

Let's Dream

735003688LD50035

3 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: Trust Care AB

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 735003688LD50035
Device name: Let's Dream
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 9, 2021

Manufacturer & authorised representative

Manufacturer

Name: Trust Care AB
SRN: SE-MF-000003384
Country: Sweden
Email: info@trustcare.se
Phone: +46 40 15 61 20

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FM1Y5VV8A1MG99K05B59SMSX

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

Let's Dream Black Swan07350036882266
Let's Dream Sunset07350036882273
Teak Chrome07350036882280