1031/M

Organization name

P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA

SRN

PT-MF-000010370

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW999

  Não utilizar em contacto com dermatoses, chagas ou feridas abertas. Certifique-se de que a área de aplicação do dispositivo se encontra seca. Caso ocorram irritações na pele, suspenda o uso e consulte o seu médico.

Primary placement in Portugal; available across 1 country total.

Trade name

not provided

UDI-DI code

05600806090165

Basic UDI-DI

560080609SEPODAF

Reference / catalog number

1031/M

Issuing entity

GS1

Risk category

Class I

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

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.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• Y061299LOWER EXTREMITY ORTHOSES - OTHER