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

00031502 — Class I MDR by PRODUCTOS FAVESAN, S.A.

MD Atlas
PRODUCTOS FAVESAN, S.A.

EUDAMED last updated this device on Apr 10, 2025

00031502

8432052PF008NU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PRODUCTOS FAVESAN, S.A.
UDI-DI code: 08432052315023
Reference / catalog number: 00031502

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

Related devices

410008432052PF011NHOn the market 000363058432052PF003NJOn the market 000360258432052PF003NJOn the market 000360208432052PF003NJOn the market 363108432052PF003NJOn 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: 08432052315023
Basic UDI-DI: 8432052PF008NU
Reference / catalog number: 00031502
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: ROLLO VERDE VISCOSA ABSORBENTE 20g 60X100
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T030502BED AND STRETCHER HYGIENIC COVERS

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