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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

10321000;137 — Class I MDR by Dr. Paul Koch GmbH

MD Atlas
Dr. Paul Koch GmbH

EUDAMED last updated this device on Nov 19, 2024

10321000;137

426043325metlagschieUQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Paul Koch GmbH
UDI-DI code: 04260433251530
Reference / catalog number: 10321000;137

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Manufacturer information

Organization name: Dr. Paul Koch GmbH
SRN: DE-MF-000006364
Manufacturer status: Active

Related devices

10320000;64426043325metlagschieUQOn the market 10320000;73426043325metlagschieUQOn the market 10320000;92426043325metlagschieUQOn the market 10322000;88426043325metlagschieUQOn the market 10322000;89426043325metlagschieUQOn the market

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260433251530
Basic UDI-DI: 426043325metlagschieUQ
Reference / catalog number: 10321000;137
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Schiene geformt, Aluminium
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03030203FOAM PADS

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.