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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

00036025 — Class I MDR by PRODUCTOS FAVESAN, S.A.

MD Atlas
PRODUCTOS FAVESAN, S.A.

EUDAMED last updated this device on Apr 10, 2025

00036025

8432052PF003NJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PRODUCTOS FAVESAN, S.A.
UDI-DI code: 08432052360252
Reference / catalog number: 00036025

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Manufacturer information

Organization name: PRODUCTOS FAVESAN, S.A.
SRN: ES-MF-000018002
Manufacturer status: Active

Related devices

410008432052PF011NHOn the market 000363058432052PF003NJOn the market 000360208432052PF003NJOn the market 363108432052PF003NJOn the market 000360658432052PF003NJOn 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.

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: 08432052360252
Basic UDI-DI: 8432052PF003NJ
Reference / catalog number: 00036025
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: BATA AZUL VISCOSA PLASTIFICADA 20g PUÑO ELASTICO 75uds
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0205NON-SURGICAL GOWNS (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE)

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

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Software identification