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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

02040-G-LIPÖDEM — Class IIa MDR by PHYSIOMED ELEKTROMEDIZIN…

MD Atlas
PHYSIOMED ELEKTROMEDIZIN AG

EUDAMED last updated this device on Jan 9, 2025

02040-G-LIPÖDEM

4099649DEEPOSZILLATION2F

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PHYSIOMED ELEKTROMEDIZIN AG
UDI-DI code: 04099649000072
Reference / catalog number: 02040-G-LIPÖDEM

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Manufacturer information

Organization name: PHYSIOMED ELEKTROMEDIZIN AG
SRN: DE-MF-000009637
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04099649000072
Basic UDI-DI: 4099649DEEPOSZILLATION2F
Reference / catalog number: 02040-G-LIPÖDEM
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: DEEP OSCILLATION Personal is a device intended for delivering transcutaneous pulsed electrostatic therapy. The function of DEEP OSCILLATION Personal is based on a pulsed electrostatic field which is built up in the patient's body region to be treated. Its frequency changes between 5 - 250 Hz, according to the selected indication. Due to the movement of the hand applicator or special glove, a vibrating or pumping effect with deep impact is induced in the patient's tissue. DEEP OSCILLATION Personal Home is a device intended for the use of laypersons in the home environment.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12062799FUNCTIONAL ELECTRICAL STIMULATION SYSTEMS - 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

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.

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