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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

1471 - GEMINI EVO — Class I MDR by Brusaferri & C. srl

MD Atlas
Brusaferri & C. srl

EUDAMED last updated this device on Nov 26, 2025

1471 - GEMINI EVO

805686022851FA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brusaferri & C. srl
UDI-DI code: 80568602203886
Reference / catalog number: LEMI MD - 2025

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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: 1471 - GEMINI EVO
UDI-DI code: 80568602203886
Basic UDI-DI: 805686022851FA
Reference / catalog number: LEMI MD - 2025
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: Multi-functional treatment table that combines comfort and ease of use. Thanks to the innovative mattress with HBS Stress Relief System, guarantees maximum comfort for both the client and practitioner alike. Equipped with three independent height, backrest and legrest adjustments and a solid painted wooden base with double column elegantly covered. IDEAL FOR: diagnostics, physiotherapy, rehabilitation, dermatology, aesthetic surgery
Additional information URL: https://www.lemimd.com/it/
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)80568602203886

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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.

V080603TREATMENT, DIAGNOSIS AND MONITORING MEDICAL BEDS

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.