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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

1157 DREAMED ZAK 4M MOVE — Class I MDR by Brusaferri & C. srl

MD Atlas
Brusaferri & C. srl

EUDAMED last updated this device on Mar 13, 2024

1157 DREAMED ZAK 4M MOVE

805686022851FA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brusaferri & C. srl
UDI-DI code: 80568602201592
Reference / catalog number: ABOUT LEMI 2024

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View device family (Basic UDI)

Manufacturer information

Organization name: Brusaferri & C. srl
SRN: IT-MF-000039891
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: 1157 DREAMED ZAK 4M MOVE
UDI-DI code: 80568602201592
Basic UDI-DI: 805686022851FA
Reference / catalog number: ABOUT LEMI 2024
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Dreamed Zak Move is equipped with highperformance and silent electronics and a practical standard foot pedal control. The shape of the backrest is designed to approach the patient face. The move base helps with cleaning and disinfection of medical environments and the base size is suitable also for small rooms. Ideal for: diagnostics, ENT, dental and ophthalmic examinations.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)80568602201592

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

V08020101GENERIC USE ELECTRIC MEDICAL CHAIRS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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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.