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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

DAVID — Class IIb MDR by metek Medizin Technik…

MD Atlas
metek Medizin Technik Komponenten GmbH

EUDAMED last updated this device on Aug 29, 2024

DAVID

426076825DAVID9A

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: metek Medizin Technik Komponenten GmbH
UDI-DI code: 04260768250000
Reference / catalog number: DAVID

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Manufacturer information

Organization name: metek Medizin Technik Komponenten GmbH
SRN: DE-MF-000006817
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: 04260768250000
Basic UDI-DI: 426076825DAVID9A
Reference / catalog number: DAVID
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Herzkatheter Messplatz mit EKG und 2 invasiven Blutdruck Messmodulen
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12050702POLYGRAPHY SYSTEMS FOR HAEMODYNAMIC STUDIES

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

DAVIDB-DAVIDYNOn 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.