Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

9474618 — Class I MDR by Greiner GmbH

MD Atlas
Greiner GmbH

EUDAMED last updated this device on Aug 10, 2022

9474618

406609846174

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Greiner GmbH
UDI-DI code: 04066098461396
Reference / catalog number: 9474618

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

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 6636300406609846174On 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	May 30, 2018	Still on market
France	May 30, 2018	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04066098461396
Basic UDI-DI: 406609846174
Reference / catalog number: 9474618
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, hydraulischem 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
Expiration date
Manufacturing date
Serial number
Software identification