Organization name

FERROX srl

SRN

IT-MF-000011243

Manufacturer status

Active

No certificate specifically references this device's Basic UDI-DI.

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

• Caution

  LEGGERE LE ISTRUZIONI PRIMA DELL'USO

Primary placement in Italy; available across 32 countries total.

Trade name

LETTINO DEGAS PRO, DELFT

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

08052532977536

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

805347043DEGAS-PROXU

Reference / catalog number

240020.91

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Lettino a due sezioni per terapia, massaggi e visite mediche, con altezza regolabile elettricamente da 50 a 92 cm tramite motore. Testiera regolabile in posizione proclive e declive mediante pistone a gas. Rivestimento e imbottitura in materiali ignifughi classe 1 IM, lavabili.

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.

• Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER

• Class I medical devices in EUDAMED