Automated Transfer Bed

Organization name

AFH Europe Sp. z o.o.

SRN

PL-MF-000039499

Manufacturer status

Active

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• CW275

  Before using the ATB, the patient must be qualified by a competent person - e.g. a Physician. The competent person should consider whether the benefits of using the device outweigh the potential risks to the patient.

Primary placement in Poland; available across 1 country total.

Placed on the market in Poland; per-country availability dates not published.

Trade name

Automated Transfer Bed

UDI-DI code

05905602641222

Basic UDI-DI

59056026412ATB052WQ

Reference / catalog number

ATB052

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

The device is intended for use in long-term care facilities. The device is not intended for use in hospitals, particularly in intensive care units.- The ATB is a stationary device and, once installed, should not be moved without a clear need. Under no circumstances should the device be transported with the patient inside it. Preparation for transporting the device is described later in this manual.The device is intended for adults with permanently or temporarily reduced motor autonomy due to disability or illness.Contraindications for the use of the device are high amputation, paresis of the shoulder girdle that prevents grasping the handle of the arms of the front platform of the device.Before using the ATB, the patient should be qualified by a competent person (doctor).The operator of the device must be trained by an authorised representative of the manufacturer.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 0–135 MU29

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

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

• Y120615POWER ASSISTED MOBILITY ROLLATORS