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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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Autohemotransfusion set — 3 UDI-DI variants, MDR (OIARSO, S. COOP)

MD Atlas
OIARSO, S. COOP

Data from EUDAMED, last updated May 23, 2026

Autohemotransfusion set

8427860AHT1100000032A8W

3 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: 8427860AHT1100000032A8W
Device name: Autohemotransfusion set
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 19, 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

3 UDI-DI variants

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Applied filters

basicUdiUlid01KM2SG1FCYHQ4F27BYVGRYAG9

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

850.0108427860850019
850.0008427860850002
850.0208427860850026