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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

G40JAS05W1 — Class I MDR by PONTE GIULIO S.P.A.

MD Atlas
PONTE GIULIO S.P.A.

EUDAMED last updated this device on May 29, 2026

G40JAS05W1

80218800000000004U5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PONTE GIULIO S.P.A.
UDI-DI code: 08023616063650
Reference / catalog number: G40JAS05W1

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View device family (Basic UDI)

Manufacturer information

Organization name: PONTE GIULIO S.P.A.
SRN: IT-MF-000010424
Manufacturer status: Active

Related devices

G40JAS24W180218800000000004U5On the market G40JAS25W180218800000000004U5On the market G40JAS01W180218800000000004U5On the market G40JAS02W180218800000000004U5On the market G40JAS03W180218800000000004U5On 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

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

CW010
Consultare istruzini d'uso
CW999
Non superare il peso massimo

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	May 29, 2026	Nov 27, 2099

Device identification

Trade name: not provided
UDI-DI code: 08023616063650
Basic UDI-DI: 80218800000000004U5
Reference / catalog number: G40JAS05W1
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: Maniglione di sicurezza per il sostegno delle persone con ridotta capacità motoria durante la fase di igiene peronale o assimilabile.
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)08023616063650

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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.

Y093399WASHING, BATHING AND SHOWERING DEVICES - 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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