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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

Vibra GO — Class IIa MDR by AD SWISS MEDTECH SA

MD Atlas
AD SWISS MEDTECH SA

EUDAMED last updated this device on Apr 15, 2026

Vibra GO

7649990376DP002FY

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: AD SWISS MEDTECH SA
UDI-DI code: 07649990376028
Reference / catalog number: DP002

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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 Slovenia; available across 1 country total.

Country	On market since	Until
SloveniaPrimary placement	Dec 10, 2025	Still on market

Device identification

Trade name: Vibra GO
UDI-DI code: 07649990376028
Basic UDI-DI: 7649990376DP002FY
Reference / catalog number: DP002
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: —
Additional information URL: No additional information URL provided by the manufacturer.
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 DP0057649990376DP005G6On 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.