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Organization name
UDI-DI code
Reference / catalog number

4223000 — Class I MDR by Greiner GmbH

MD Atlas
Greiner GmbH

EUDAMED last updated this device on Aug 8, 2022

4223000

40660984226S

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Greiner GmbH
UDI-DI code: 04066098422014
Reference / catalog number: 4223000

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Manufacturer information

Organization name: Greiner GmbH
SRN: DE-MF-000007660
Manufacturer status: Active

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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.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Jun 16, 2016	Still on market
France	Jun 16, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04066098422014
Basic UDI-DI: 40660984226S
Reference / catalog number: 4223000
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 Dialyseliege Multiline Next DC wurde als Therapieliege für den Einsatz während einer Dialysebehandlung entwickelt. Sie kann zum Patiententransport innerhalb von Gebäuden eingesetzt werden. Die Liege ist ausschließlich für den Einsatz in Gebäuden und bei normalen Umgebungsverhältnissen vorgesehen.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08020101GENERIC USE ELECTRIC MEDICAL CHAIRS

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

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Manufacturing date
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