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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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RUTILIGHT — 2 UDI-DI variants, MDR (SWAN MEDICAL, S.L)

MD Atlas
SWAN MEDICAL, S.L

Data from EUDAMED, last updated May 23, 2026

RUTILIGHT

8437016917RL-013P

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SWAN MEDICAL, S.L

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8437016917RL-013P
Device name: RUTILIGHT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: SWAN MEDICAL, S.L
SRN: ES-MF-000001526
Country: Spain
Email: admin@swanmedical.es
Phone: +34 938 32 58 97

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HF6H03GJ14XJ9DKCH04JXTWG

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

RL-0108437016917350
RL-0108437016917176