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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

PhysioSensing Rehab — Class I MDR by Sensing Future…

MD Atlas
Sensing Future Technologies

EUDAMED last updated this device on Sep 3, 2025

PhysioSensing Rehab

56001138337PRESSPLT32

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sensing Future Technologies
UDI-DI code: 05600113833721
Reference / catalog number: PhysioSensing Rehab

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View device family (Basic UDI)

Manufacturer information

Organization name: Sensing Future Technologies
SRN: PT-MF-000028345
Manufacturer status: Active

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW016
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Portugal; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05600113833721
Basic UDI-DI: 56001138337PRESSPLT32
Reference / catalog number: PhysioSensing Rehab
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: —
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)05600113833721

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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.

Z12062603SENSOR-BASED PLATFORMS

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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Related devices

II REHAB56001138337PRESSPLT32On the market III MAX REHAB56001138337PRESSPLT32On the market IV VERTIGO56001138337PRESSPLT32On the market PhysioSensing Posturography56001138337FORCEPLTQ5On the market PhysioSensing Basic56001138337FORCEPLTQ5On 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.