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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

6115-00-00-00 — Class I MDR by Jörg & Sohn GmbH

MD Atlas
Jörg & Sohn GmbH

EUDAMED last updated this device on Feb 13, 2023

6115-00-00-00

42517328OPTW9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Jörg & Sohn GmbH
UDI-DI code: 04251732800055
Reference / catalog number: 6115-00-00-00

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Manufacturer information

Organization name: Jörg & Sohn GmbH
SRN: DE-MF-000011346
Manufacturer status: Active

Related devices

9121-26-00-0042517328912126-2D-OSNBOn the market 6124-02-00-0042517328ACCRSOn the market 6120-00-0042517328OPTW9On the market 612642517328OPTAKM4On the market 6124-03-00-0042517328ACCRSOn 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: 04251732800055
Basic UDI-DI: 42517328OPTW9
Reference / catalog number: 6115-00-00-00
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: Die OP-Tische sind für die Positionierung des Patienten während der Operation vorgesehen und reicht von der Einleitung der Anästhesie über die eigentliche Operation bis zur Wiederherstellung nach der Anästhesie ebenso wie der Patiententransport und die Operationstischplatte, von einer Patiententransfereinheit zum Operationssaal oder vom Operationssaal zur Patienten Transfereinheit.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12011202OPERATING TABLES

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.