Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

850.02 — Class IIa MDR by OIARSO, S. COOP

MD Atlas
OIARSO, S. COOP

EUDAMED last updated this device on Mar 27, 2026

850.02

8427860AHT1100000032A8W

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OIARSO, S. COOP
UDI-DI code: 08427860850026
Reference / catalog number: 850.02

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: OIARSO, S. COOP
SRN: ES-MF-000000866
Manufacturer status: Active

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW007
Do not use if the outer packaging is damaged or incomplete.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW999
1. No utilizar si el envase está deteriorado o no está íntegro. 2. No reutilizar ni reesterilizar

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 26, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08427860850026
Basic UDI-DI: 8427860AHT1100000032A8W
Reference / catalog number: 850.02
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: AUTOHEMOTRANSFUSION SET
Additional information URL: https://bexen.com/biblioteca/#anchor-des-instrucciones
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

B0499AUTOTRANSFUSION DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

158.028427860SFP2100000022ASQOn the market 850.078427860CAR10010000510X5On the market 137.03B-ESMF00000086613703DDOn the market 091.03B-ESMF00000086609103DEOn the market 850.098427860STF1100000021AY2On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.