SACCONANNA

Organization name

Storello Ausili SRL

SRN

IT-MF-000045673

Manufacturer status

Active

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

• CW010

  Use only under supervision of trained healthcare personnel or caregiver. Not intended as a substitute for patient monitoring. Assess patient suitability before use; contraindicated in patients whose clinical condition is incompatible with restraint systems. Do not use if the device is damaged or improperly installed. Incorrect use may result in injury or compromise patient safety.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

08054953810881

Basic UDI-DI

805495381CONT_LETTOXJ

Reference / catalog number

SACCONANNA

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

Device intended to ensure patient safety during bed rest by limiting uncontrolled movements and preventing accidental falls or unassisted attempts to leave the bed. Suitable for use in healthcare, assistance and home care settings under supervision of trained personnel.

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.

• M030599IMMOBILISATION SYSTEMS AND DEVICES - OTHER