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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

2207302 — Class I MDR by Greiner GmbH

MD Atlas
Greiner GmbH

EUDAMED last updated this device on Aug 8, 2022

2207302

40660982206C

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Greiner GmbH
UDI-DI code: 04066098220016
Reference / catalog number: 2207302

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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	Jul 26, 2010	Still on market
France	Jul 26, 2010	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04066098220016
Basic UDI-DI: 40660982206C
Reference / catalog number: 2207302
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: Blutabnahmestuhl/Patientensessel mit Integralschaum-Armlehnen, zusätzlicher Blutabnahmearmlehne (als Option) und diversen Stuhlunterteilen. Rückenneigung mittels Gasfeder.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080202MANUAL 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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Software identification