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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

DP005 — Class IIa MDR by AD SWISS MEDTECH SA

MD Atlas
AD SWISS MEDTECH SA

EUDAMED last updated this device on May 13, 2026

DP005

7649990376DP005G6

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AD SWISS MEDTECH SA
UDI-DI code: 07649990376059
Reference / catalog number: DP005

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Manufacturer information

Organization name: AD SWISS MEDTECH SA
SRN: CH-MF-000037918
Manufacturer status: Active

Critical warnings

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

CW011
READ ALL INSTRUCTIONS

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	May 13, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07649990376059
Basic UDI-DI: 7649990376DP005G6
Reference / catalog number: DP005
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: PONOS is a non-invasive physical therapy medical device intended for pain treatment and support of rehabilitation processes through the transcutaneous application of physical energies via electrodes applied to the skin. The devices are intended for use in the treatment of painful conditions of musculoskeletal and neuropathic origin within the fields of physical and rehabilitation medicine, physiatry, orthopedics, and pain therapy.
Additional information URL: https://www.neuromodulationsystem.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12062899NEUROMUSCULAR STIMULATION EQUIPMENT - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

DP0037649990376DP003G2On the market DP0067649990376DP006G8On the market DP0017649990376DP001FWOn the market Vibra GO7649990376DP002FYOn 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.