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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

6636300 — Class I MDR by Greiner GmbH

MD Atlas
Greiner GmbH

EUDAMED last updated this device on Aug 8, 2022

6636300

406609846174

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Greiner GmbH
UDI-DI code: 04066098461297
Reference / catalog number: 6636300

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Manufacturer information

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

Related devices

6736308406609846174On the market 6636200406609846174On the market 6736208406609846174On the market 6632000406609846174On the market 6612085406609846174On 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.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Nov 23, 2017	Still on market
France	Nov 23, 2017	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04066098461297
Basic UDI-DI: 406609846174
Reference / catalog number: 6636300
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: Untersuchungs- und Behandlungsstuhl mit mechanisch oder elektromechanisch verstellbarem Unterteil, Oberteil wahlweise mit Gasfeder oder elektromechanisch verstellbar.
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

Batch number
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Software identification