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On 25 May 2017 was announced that the transitional period of MDR will end on the 26 May 2020. The new Medical Device Regulation (MDR), also called the European Medical Device Regulation, should have came into force across Europe by the 26 May 2020. Due to the corona pandemic, the EU Commission has now decided to set 26 May 2021 as the amended date of implementation of the MDR.
Memmert has already successfully passed the extension of the MDD 93/42/EEC certificates. Memmert successfully has passed the extension of the MDD 93/42/EEC certificates. The existing EC certificate, directive 93/42/EEC was issued by the notified body and is now valid until May 2024 according to
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. Occurrence Report Customer Occurrence report which needs to be sent by the customer in case there is
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
Here are all temperature control appliances that are classified as medical devices according to the Medical Device Directive for Clinic & Pharmacy.
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 13485 certified since many years. The following products are classified as medical device. Me
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 will find the intended purpose for all Memmert ovens classified as medical devices.
Intended purpose Medical devices Memmert successfully has passed the extension of the MDD 93/42/EEC certificates. The existing EC certificate, directive 93/42/EEC was issued by the notified body and is now valid until May 2024 according to the transitional regulation (EU) 2017/745. The direct
Blanket warmers are vital when giving first aid to seriously injured patients in emergency rooms. In a Memmert blanket warmer IFbw, blankets and cloths preheated to any precise temperature to keep patients warm before and after surgery are always close at hand. This minimises the risk of complications such as wound infections, cardiovascular disorders, cardiac arrhythmia or vascular disorders.
After the Memmert CO 2 incubator ICOmed was recently classified as a medical device, this is now followed by the blanket warmers IFbw . These appliances are Class I medical devices in accordance with EU Directive 93/42/EEC and are intended for warming non-sterile blankets and cloths. A str
Memmert service and download area with online forms as well as brochures, flyers, user manuals and software.
Service Online form for messages to the Memmert technical service 24 hours a day. Medical Devices Medical devices are subject to special statutory regulations. Here you will find all the necessary documents.
Technical Support Here you will find important telephone numbers and email addresses for our technical support as well as forms for service messages and spare parts enquiries. Contact Technical Service Service Report Customer Service Report Distributor Spare parts