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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

S002 — IVDR Class A IVDR by Vircell, S.L

MD Atlas
Vircell, S.L

EUDAMED last updated this device on Dec 27, 2022

S002

843604032S00201QB

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Vircell, S.L
UDI-DI code: 08436040325285
Reference / catalog number: S002

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Manufacturer information

Organization name: Vircell, S.L
SRN: ES-MF-000004099
Manufacturer status: Active

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Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08436040325285
Basic UDI-DI: 843604032S00201QB
Reference / catalog number: S002
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0599IVD GENERAL USE CONSUMABLE DEVICES - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Expiration date
Manufacturing date
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Software identification

Certificates

Certificate health across this manufacturer's portfolio.

V13 112727 0005Supplemented
Quality management systemNotified body: 0123Expiry: Oct 17, 2027