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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
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-
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
The heating oven Um is a Class I medical device.
Memmert heating ovens Um or Umplus may be used for heating fango, silicate and APS packs for physical therapy and keeping them warm. Memmert is bringing medical devices of class I according to the regulation MDR (EU) 2017/745 into circulation. The heating oven Um is a Class I medical device.
The incubator Im is a Class I medical device.
Incubators Im and Implus may be used for temperature control of rinsing, infusion solutions, and contrast agents. With the fine-tuned control technology, critical temperature overshoots are completely ruled out. Rinsing and infusion solutions are therefore heated precisely and particularly gently in The incubator Im is a Class I medical device.

UN160mplus Model

The heating oven Um is a Class I medical device.
Um 160 * The heating oven Um is a Class I medical device.

UN160m Model

The heating oven Um is a Class I medical device.
Um 160 * The heating oven Um is a Class I medical device.

UF110mplus Model

The heating oven Um is a Class I medical device.
Um 110 * The heating oven Um is a Class I medical device.