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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

47 — Class I MDR by ORMESA S.r.l.

MD Atlas
ORMESA S.r.l.

EUDAMED last updated this device on Jul 31, 2025

47

805571570BUGL9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ORMESA S.r.l.
UDI-DI code: 08055715702932
Reference / catalog number: 47

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View device family (Basic UDI)

Manufacturer information

Organization name: ORMESA S.r.l.
SRN: IT-MF-000034824
Manufacturer status: Active

Related devices

47805571570BUGL9On the market 47805571570BUGL9On the market 47805571570BUGL9On the market 47805571570BUGL9On the market 47805571570BUGL9On 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.

CW030
The device must be prescribed and / or configured and adjusted by a rehabilitation professional according to the laws in the user's place of residence

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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: 08055715702932
Basic UDI-DI: 805571570BUGL9
Reference / catalog number: 47
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: https://www.ormesa.com/
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.

Y180939MODULAR POSTURE SYSTEMS

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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