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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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Solution filter — 4 UDI-DI variants, MDR (OIARSO, S. COOP)

MD Atlas
OIARSO, S. COOP

Data from EUDAMED, last updated May 23, 2026

Solution filter

8427860SFP2100000022ASQ

4 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: OIARSO, S. COOP

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8427860SFP2100000022ASQ
Device name: Solution filter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: OIARSO, S. COOP
SRN: ES-MF-000000866
Country: Spain
Email: info@bexenmedical.com
Phone: +34 943 33 50 20

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKECA0R6YAAPYRNV6X5XQAZ0

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

158.0208427860158023
157.1208427860157125
157.0208427860157026
158.1208427860158122