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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

VAS-07STRONG — Class IIa MDD by EMBITRON s.r.o.

MD Atlas
EMBITRON s.r.o.

EUDAMED last updated this device on May 19, 2026

VAS-07STRONG

B-08596526112003

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: EMBITRON s.r.o.
UDI-DI code: 08596526112003
Reference / catalog number: VAS-07STRONG

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Manufacturer information

Organization name: EMBITRON s.r.o.
SRN: CZ-MF-000041086
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 Czechia; available across 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08596526112003
Basic UDI-DI: B-08596526112003
Reference / catalog number: VAS-07STRONG
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The purpose of the device VAS-07 Edition “Better Future”, variant Strong, is to provide induced low frequency pulses and mid-frequency interference electrotherapy currents without the need to apply contact electrodes to the patient’s body in order to have a positive therapeutic effect on painful conditions and to promote healing, regeneration or repair of musculoskeletal tissues.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120601ELECTROTHERAPY EQUIPMENT (INCLUDED TENS)

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

VAS-07BASICB-08596526111006On the market EXTREMITER2020B-08596526110009On 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.