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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

Materasso serie Fisio Form… — Class I MDR by AP GROUP SRL

MD Atlas
AP GROUP SRL

EUDAMED last updated this device on Jul 2, 2025

Materasso serie Fisio Form 80x190x12

805559896FISIONW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AP GROUP SRL
UDI-DI code: 08055598960177
Reference / catalog number: 08055598960177

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View device family (Basic UDI)

Manufacturer information

Organization name: AP GROUP SRL
SRN: IT-MF-000048451
Manufacturer status: Active

Related devices

Guanciale serie Fisiopharm 500x800x100805559896FISIONWOn the market Guanciale serie Fisiopharm 500x800x120805559896FISIONWOn the market Guanciale serie Fisiopharm 500x800x40805559896FISIONWOn the market 08055598960238805559896FISIONWOn the market 08055598960207805559896FISIONWOn the market

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.

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: Materasso serie Fisio Form 80x190x12
UDI-DI code: 08055598960177
Basic UDI-DI: 805559896FISIONW
Reference / catalog number: 08055598960177
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: materasso dotato di lastra interna con bordo di contenimento, sicurezza e sostegno realizzata in poliuterano espanso 30FP del tipo polietere ad alta risposta elastica _8densità 30 kg / m3). superficie di appogiio in memory foam automodellante VE 50 AU altamente traspirante (densità 50 kg / m3)
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)08055598960177

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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.

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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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