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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

DMHDR100 — Class I MDR by Sensor Medica Srl

MD Atlas
Sensor Medica Srl

EUDAMED last updated this device on Dec 18, 2025

DMHDR100

8052015180200SM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sensor Medica Srl
UDI-DI code: 08052015180200
Reference / catalog number: DMHDR100

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View device family (Basic UDI)

Manufacturer information

Organization name: Sensor Medica Srl
SRN: IT-MF-000032343
Manufacturer status: Active

Related devices

DMHDR2508052015180231SYOn the market DMHDR1508052015180217T6On the market DMHDR2008052015180224T3On the market DMHDR3008052015180248THOn the market Gomedic 2D8052015181047TCOn 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
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: not provided
UDI-DI code: 08052015180200
Basic UDI-DI: 8052015180200SM
Reference / catalog number: DMHDR100
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: Sistema di valutazione dell'appoggio plantare per analisi statica e dinamica
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)08052015180200

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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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