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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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Sunrise sensor — 2 UDI-DI variants, MDR (Sunrise SA)

MD Atlas
Sunrise SA

Data from EUDAMED, last updated May 23, 2026

Sunrise sensor

5430001896SunriseDxSenQU

2 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: Sunrise SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5430001896SunriseDxSenQU
Device name: Sunrise sensor
Device model: SUN100
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 1, 2023

Manufacturer & authorised representative

Manufacturer

Name: Sunrise SA
SRN: BE-MF-000000105
Country: Belgium
Email: support@hellosunrise.com
Phone: +3281261126

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GZBBNTD1D6VF3Q02S5Y4B36Q

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

Sunrise sensor05430001896121
Sunrise sensor05430001896008