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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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Organization name
UDI-DI code
Reference / catalog number

61009 — IVDD — General IVDD by BIOSYSTEMS S.A.

MD Atlas
BIOSYSTEMS S.A.

EUDAMED last updated this device on Oct 22, 2025

61009

B-08435287106503

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: BIOSYSTEMS S.A.
UDI-DI code: 08435287106503
Reference / catalog number: 61009

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Manufacturer information

Organization name: BIOSYSTEMS S.A.
SRN: ES-MF-000000231
Manufacturer status: Active

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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.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement	Nov 29, 2013	Still on market
Italy	Nov 29, 2013	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08435287106503
Basic UDI-DI: B-08435287106503
Reference / catalog number: 61009
Issuing entity: GS1

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: See IFU (section intended use)
Additional information URL: https://einfo.bio/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103020102ACTIVATED PARTIAL THROMBOPLASTIN TIME

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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