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Share Name | Share Symbol | Market | Type | Share ISIN | Share Description |
---|---|---|---|---|---|
Bactiguard Holding Ab | LSE:0QV2 | London | Ordinary Share | SE0005878741 | BACTIGUARD HOLDING ORD SHS |
Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
---|---|---|---|---|---|---|---|---|---|---|
0.00 | 0.00% | 24.10 | 0.00 | 01:00:00 |
Industry Sector | Turnover | Profit | EPS - Basic | PE Ratio | Market Cap |
---|---|---|---|---|---|
Health & Allied Services,nec | 223.17M | -138.38M | -4.4576 | -5.41 | 748.16M |
STOCKHOLM, Jan. 10, 2023 /PRNewswire/ -- Bactiguard today announces its first MDR (Medical Device Regulations 2017/745) product approval following a comprehensive authorization process. The MDR approval relates to the latex BIP Foley Catheter which is an indwelling urinary catheter with Bactiguard's unique infection prevention technology.
Bactiguard's patented technology is based on a thin noble metal alloy coating attached to the catheter surface. When in contact with fluids, the metals create a galvanic effect which reduces microbial adhesion where fewer bacteria adhere to the catheter surface. Today, one out of ten patients worldwide are affected by healthcare associated infections (HAI) and catheter-associated urinary tract infections (CAUTI) stand for a considerable part. Urinary catheters with Bactiguard's technology reduce the risk of CAUTI significantly.
- Patient safety always comes first for Bactiguard, and stricter regulations are an advantage to us. Products scrutinized in the MDR-process are audited through higher standards of quality and safety. The BIP Foley catheter made it through this thorough process and will not only improve patient safety by reducing the risk of HAI but also by reducing the use of antibiotics. A powerful combination with positive impact on both patients and a healthier world, says Fatima Stensvad Flodin, Bactiguard's Chief Quality & Regulatory Officer.
The new MDR regulations were adopted as per May 26, 2021, to ensure that only non-harmful equipment used on patients and by care takers is allowed on the European market. The regulatory landscape is complex and Bactiguard will continue to carefully monitor various new demands and requirements, set by both the market and regulatory agencies, on medical devices.
For more information, please contact:
Bactiguard press office +46 8 440 58 80 info@bactiguard.co
The following files are available for download:
https://mb.cision.com/Main/9686/3695096/1770001.pdf | 230110 Bactiguard receives first MDR product approval |
https://news.cision.com/bactiguard-holding-ab--publ-/i/bip-foley-catheter,c3131563 | BIP Foley Catheter |
View original content:https://www.prnewswire.co.uk/news-releases/bactiguard-receives-first-mdr-product-approval-301717494.html
Copyright 2023 PR Newswire
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