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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 Incident Report Customer Incident report which needs to be sent by the customer in case there is any trouble with your Memmert medical device. Incident Report Dealer Incident report which needs to be sent by the distributor in ca
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
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
The Memmert CO 2 incubator ICOmed now is a class IIa medical device for in-vitro fertilisation and biosynthesis. The CE label on the appliances includes the mark 0197, denoting TÜV Rheinland LGA Products GmbH as the notified body.
In 2016, Memmert had introduced a new generation of its CO 2 incubators at the analytica trade show. Now, about one year later, all products in the ICOmed product range have been classified as medical devices. "Hospitals and medical practices from all around the world that have specialized in in-
Here you find all products classified as medical device according to the medical device directive (93/42/EEC).
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. The following products are classified as medical device ac

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.

IF260bw Model

The Memmert blanket warmer IFbw is a Class I medical device in accordance with the EU Directive 93/42/EEC.
IF260bw The Memmert blanket warmer IFbw is a Class I medical device in accordance with the EU Directive 93/42/EEC.

IF110bw Model

The Memmert blanket warmer IFbw is a Class I medical device in accordance with the EU Directive 93/42/EEC.
IF110bw The Memmert blanket warmer IFbw is a Class I medical device in accordance with the EU Directive 93/42/EEC.