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Here you will find the intended purpose for all Memmert ovens classified as medical devices as well as the respective form in case of sending an incident report when having issues with a Memmert medical device.
Memmert as medical device Intended purpose as medical device Here you will find the intended purpose for all Memmert ovens classified as medical devices. Incident Report Customer Incident report which needs to be sent by the customer in case there is any
As of now, the Memmert CO 2 incubator INCO is recognised as a class IIa medical device for in vitro fertilization and gene expression. In addition to the CE mark, the devices are labelled with the number 1275, identifying LGA InterCert GmbH as the notified body.
Hardly any field of medicine moves us like reproductive medicine does. In the sterile and highly sophisticated environment of an IVF laboratory, new life is created, making it a matter of course that the quality requirements to be met there are extremely strict, in order to protect the sensitive ova
Here you will find the intended purpose for all Memmert ovens classified as medical devices.
Intended purpose Medical devices For ovens covered by the scope of the Directive 93/42/EWG (Directive of the Commission on the harmonization of the legal regulations of the Member States on medical devices) the following intended purpose applies:

Service Page

Online form for messages to the Memmert technical service 24 hours a day.
Service report Online form for messages to the technical service 24 hours a day. Service Report Customer Service Report Distributor Medical devices Here you will find the intended purpose for all Memmert ovens classified as medical devices as
Incident report which needs to be sent by the distributor in case there is any trouble with your Memmert medical device.
Incident report which needs to be sent by the customer in case there is any trouble with your Memmert medical device.
For different reasons, Memmert has to undergo a recertification process every three years in accordance with the worldwide strictest quality management system for medical devices DIN EN ISO 13485. The most important reason is clear: highest possible safety for our clients.
Safety check # 1: ISO 13485 In many aspects, the DIN EN ISO 13485:2012, as it is called in its current version, is congruent with the international standard for quality management, the DIN EN ISO 9001. Compared to the latter however, it sets out additional requirements such as, among other thi

Medicine Sector

It is our hard-lined commitment to quality that has made Memmert a reliable partner in the medical sector and medical research industry ever since the company’s founding in 1947. Of course we are DIN EN ISO 13 485 certified since many years. This medical applications special introduces suitable appliances as well as case studies.
It is our passion for details that makes Memmert heating ovens, incubators and waterbaths so precise and durable. The fact that all of our products are developed and manufactured exclusively in-house has made us technology leaders in temperature control appliances. It is our hard-lined commitment to It is our hard-lined commitment to quality that has made Memmert a reliable partner in the medical sector and medical research industry ever since the company’s founding in 1947. Of course we are DIN EN ISO 13 485 certified since many years. This medical applications special introduces suitable appliances as well as case studies.
The cleanroom-compliant drying oven for microelectronics, medical technology, pharmaceutics and food technology.
The suitability of the Memmert universal oven UF750plus for use in the cleanroom has been confirmed by the independent Fraunhofer IPA (Institute for Manufacturing Engineering and Automation). It is therefore entitled to bear the certificate Fraunhofer TESTED DEVICE® . In order to guarantee the ma The cleanroom-compliant drying oven for microelectronics, medical technology, pharmaceutics and food technology.
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