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EUDAMED last updated this device on May 21, 2026
B-06959809601878Patient Programmer Recharger is an AIMDD-legacy active implantable device registered in EUDAMED. It is classified as AIMDD. Manufactured by Beijing PINS Medical Co., Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06959809601878R801(01)06959809601878
European Medical Device Nomenclature — the EU product classification assigned to this device.
J020199CEREBRAL IMPLANTABLE NEUROSTIMULATORS - OTHER1 warning recorded — scroll inside the panel to see all entries.
CN-MF-000022865CE 618912CE 618911Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | 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.B-06959809601816On the marketImplantable Lead Kit for Deep Brain StimulationB-06959809601830On the marketPatient ProgrammerB-06959809601861On the marketSingle Channel Implantable Pulse Generator Kit for Deep Brain StimulationB-06959809601793On the marketTest Extension Kit for Deep Brain StimulationB-06959809601854On the marketTest StimulatorB-06959809601892On the market