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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

72O — IVDR Class A IVDR by ENVASES FARMACÉUTICOS,…

MD Atlas
ENVASES FARMACÉUTICOS, S.A.

EUDAMED last updated this device on Dec 23, 2022

72O

8431785UDI-DI-086V

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: ENVASES FARMACÉUTICOS, S.A.
UDI-DI code: 08431785003702
Reference / catalog number: 72O

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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 72U8431785UDI-DI-076TOn the market

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: 08431785003702
Basic UDI-DI: 8431785UDI-DI-086V
Reference / catalog number: 72O
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: Recipiente cilíndrico de boca ancha, paredes semitransparentes, flexible e impermeable. Posee asa que no sobresale del cuerpo cilíndrico, facilitando su utilización. Cierre hermético, provisto de tapa a rosca y obturador que ajusta a presión. Cuerpo graduado cada 50ml hasta los 2000 ml
Additional information URL: https://eifu.enfa.es/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W050301029099SAMPLES ANALYSES, PLASTIC CONTAINERS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
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Software identification

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.