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Organization name
UDI-DI code
Reference / catalog number

MV-2020-102 — Class IIb MDD by Gerhard Müller Medizin…

MD Atlas
Gerhard Müller Medizin Technik e.K.

EUDAMED last updated this device on May 7, 2026

MV-2020-102

B-04262435280006

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Gerhard Müller Medizin Technik e.K.
UDI-DI code: 04262435280006
Reference / catalog number: MV-2020-102

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Manufacturer information

Organization name: Gerhard Müller Medizin Technik e.K.
SRN: DE-MF-000016354
Manufacturer status: Active

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: 04262435280006
Basic UDI-DI: B-04262435280006
Reference / catalog number: MV-2020-102
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: MukoStar®VibraJet®: ist für folgende Zwecke gedacht: - dient zur mechanischen Unterstützung der Schleimlösung in der Lunge, - dient zur Unterstützung der mukoziliären Clearance, - dient der Reduzierung von Instabilitäten der Frequenz und der Impulsintensität durch Druckveränderungen im System im Gegensatz zu Systemen mit anderer - Technologie, - dient der Bediensicherheit durch eine dem Therapieverlauf angepasste Bedienung, - dient dazu, eine therapiekonforme, angepasste sichere Klimatisierungsleistung durch eine angepasste Flowsteuerung zu ermöglichen, - dient dazu eine vom Versorgungsdruck weitestgehend unabhängige Therapieeinstellung zu ermöglichen. Patientenanwendungsteil: In Verbindung mit dem MukoStar®VibraJet® für die Behandlung mit Intratoracaler Percussions Ventilation IPV.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z1203019099VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT – 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

This device is not currently linked to any other device.

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.