According to EU officials, EU environmental ministers on Monday failed to reach a consensus on the approval of a genetically modified rapeseed. This is also the ninth EU stalemate on biotechnology food approval. Among the 25 EU ministers, the number of people who support or oppose the approval of GT73 rapeseed has not reached the majority. GT73 Rapeseed is a genetically modified product that is produced and marketed by Monsanto, an American biotechnology company. EU officials said that the ball is currently being kicked back to the European Commission and may be held in January next year, decided by the European Commission. The exact date depends on the time required to complete the relevant paperwork. Although there was no formal vote, the ministers stated that they insisted on their respective positions on GT73. Among the 25 member states, representatives from 6 member states agreed to approve GM rapeseed, which is France, Finland, Portugal, Slovakia, Sweden and the Netherlands. Ireland, Slovenia, Spain, Germany, Britain and the Czech Republic stated that they will abstain. The remaining countries expressed their opposition to the approval of GM rapeseed. The purpose of Monsanto's application is to allow GT73 rapeseed to be used for animal feed and processing in the EU, excluding sowing. GT73 genetically modified rapeseed is genetically modified to resist non-selective herbicides, so farmers can increase the efficiency of weed control. According to the EU's complex decision-making process, if the EU member states fail to reach a decision after the ministerial meeting to allow GM foods to enter the EU, the EU commission will make a decision to grant authorization. This will also be the third GM product that the European Union can approve to import from May 2004.
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Disposable minimally invasive fascial closure device is a medical device used to close the abdominal fascia layer after laparoscopic surgery. The device consists of a needle and suture that can be inserted through a small incision in the skin and used to close the layers of fascia without the need for a larger incision. The device is designed to reduce the risk of complications associated with traditional methods of fascial closure, such as wound infection, hernia and dehiscence. The single-use nature of the device also reduces the risk of cross-contamination and infection. Use of the device could shorten recovery time and improve outcomes for patients undergoing laparoscopic surgery.
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