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EUDAMED last updated this device on Mar 17, 2026
7649990376DP001FWVibra 3.0 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by AD SWISS MEDTECH SA. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
07649990376011DP001(01)07649990376011
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12062899NEUROMUSCULAR STIMULATION EQUIPMENT - OTHER2 warnings recorded — scroll inside the panel to see all entries.
The DP001 Vibra 3.0 medical device is suitable for use in all professional environments suitable for medical use with the exception of installations in the vicinity of HF surgical equipment and
CH-MF-000037918The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Poland; available across 6 countries total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Mar 20, 2025 | Still on market |
| Germany | Feb 5, 2026 | Still on market |
| Spain | Jan 14, 2026 | Still on market |
| Italy | May 22, 2025 | Still on market |
| Portugal | Feb 6, 2026 | Still on market |
| Romania | Apr 15, 2025 | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
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.