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Organization name
UDI-DI code
Reference / catalog number

POSEIDONE COUCH — Class I MDR by FISIOTECH srl

MD Atlas
FISIOTECH srl

EUDAMED last updated this device on May 24, 2024

POSEIDONE COUCH

8050593941117ASN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FISIOTECH srl
UDI-DI code: 80505939416886
Reference / catalog number: 1117A

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Manufacturer information

Organization name: FISIOTECH srl
SRN: IT-MF-000028185
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.
CW257
EUDAMED did not publish a description for this code.

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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: POSEIDONE COUCH
UDI-DI code: 80505939416886
Basic UDI-DI: 8050593941117ASN
Reference / catalog number: 1117A
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: Lettino POSEIDONE per RPG a quattro segmenti regolabile elettricamente in altezza da cm. 56 a cm. 100 mediante comando a pedale, pedaliera circolare. Pediera regolabile da +60° a -90° mediante pistone a gas. Appoggia braccia che scorrono su tutta la lunghezza del piano fisso e ruotano di 180°. Piano imbottito e rivestito in similpelle lavabile ed ignifugo classe 1 IM. Portata max 200 Kg.
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

EMDN nomenclature code(s)

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

Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER

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.