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

C11 — Class I MDR by ENVASES FARMACÉUTICOS,…

MD Atlas
ENVASES FARMACÉUTICOS, S.A.

EUDAMED last updated this device on May 21, 2026

C11

8431785UDI-DI-016F

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ENVASES FARMACÉUTICOS, S.A.
UDI-DI code: 08431785003115
Reference / catalog number: C11

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: ENVASES FARMACÉUTICOS, S.A.
SRN: ES-MF-000000902
Manufacturer status: Active

Related devices

72F8431785UDI-DI-076TOn the market 72G8431785UDI-DI-076TOn the market 72P8431785UDI-DI-076TOn the market 72D8431785UDI-DI-076TOn the market 72O8431785UDI-DI-086VOn 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.

Country	On market since	Until
SpainPrimary placement	Jan 1, 2015	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08431785003115
Basic UDI-DI: 8431785UDI-DI-016F
Reference / catalog number: C11
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: Finalidad Para la recogida de orina y/o heces en pacientes encamados o con movilidad reducida. Destinada al uso hospitalario y/o domiciliario. Descripción Orinal en forma de cuña, con paredes bajas, bordes redondeados y asa en forma de “L”, para fácil manejo y transporte. Capacidad: 2000 ml Peso neto: 435 g Altura máxima: 93 mm Largo máximo: 430 mm Ancho máximo: 267 mm Composición Polipropileno copolímero y colorante blanco.
Additional information URL: https://eifu.enfa.es/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0812FECES AND URINE COLLECTION AIDS (BED PANS AND PARROTS)

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