medical sterilization News
-
What is the manufacturing process flow of medical sterilization packaging bags?
The manufacturing process of medical sterilization packaging bag includes the upper film and the base paper, which is characterized in that a circle of water-based adhesive is coated on the four frames of the back of the base paper, and the back paper and the upper film are heated at the position where the water-based adhesive is coated on the back of the paper to form a medical sterilization ...
-
03How to select medical sterilization bags
Some important considerations when purchasing medical sterilization bags: Try to buy items in the same place. If you buy sterilization bags, tooth cleaning cloth, masks, tooth cloth, impression materials and other items in different places, it will take a lot of time. During the economic crisis, if customers lose their jobs, they may also lose their medical insurance, which means that they will ...
-
Specification and usage of disposable medical sterilization bag
The medical sterilization bag is a medical device approved by the Food and Drug Administration. The appearance of the sterilizing bag must be able to penetrate the sterilizing agent and provide protection during handling and storage. Therefore, a properly used sterilizing bag will provide an effective barrier against contamination before reuse. It is a self sealing paper/transparent plastic ...
-
Analysis of medical sterilization packaging bag
Disinfection and sterilization packaging can be divided into two parts: primary packaging and auxiliary packaging. Generally speaking, the disinfection and sterilization packaging of medical devices refers to the initial packaging of the product, that is, the part that directly contacts the product and forms a microbial barrier. Auxiliary packaging mainly involves the storage and circulation of ...
-
Common problems and countermeasures in the production of medical sterilized paper plastic packaging bags
The medical sterilization paper plastic packaging bag is a disposable medical sterilization packaging material, which has the advantages of good air permeability, good penetration of sterilization medium, high bacteria resistance after sterilization, convenient chemical monitoring during sterilization, simple package sealing, good perspective, long safety period after sterilization, easy opening, ...
-
SteriLux closes new financing round
SteriLux, the Swiss medical technology startup that took the step from product development to market entry this year, announces the closing of a CHF 1.78M financing round completed in December 2019. In addition to existing investors, the cooperative ONE CREATION as well as new private investors are joining this financing round. This investment will support the launch of the first product as well ...
By SteriLux SA
-
Selection of medical packaging materials
Medical packaging materials can be divided into two categories: reusable packaging materials and disposable packaging materials. Packaging begins with the selection of appropriate packaging materials and methods. In addition to the sterilization method, the packaging method should also consider the sterilization items. People have done a lot of research on this, and many kinds of medical ...
-
BioQ Pharma to Present at the 38th Annual Canaccord Genuity Growth Conference
BioQ Pharma Incorporated, a specialty pharmaceutical company, announced today that the Company will be presenting at the 38th Annual Canaccord Genuity Growth Conference to be held in Boston Massachusetts on August 8th and 9th, 2018. Josh Kriesel, President and Chief Executive Officer, is scheduled to present on Wednesday, August 8th at 12:30 p.m. Eastern Daylight Time. About BioQ Pharma BioQ ...
By BioQ Pharma
-
STEMart Launches Bioburden and Sterility Testing for Medical Devices
STEMart, a U.S.-based provider of comprehensive services for all stages of medical device development, has recently introduced the Bioburden and Sterility Testing services for medical devices under the guidance of the ISO 11731 method. For medical device manufacturers, sterility assurance is a vital part in producing safe products. The FDA and other regulatory agencies require validation of ...
By STEMart
-
BioQ Pharma Announces Positive Closure of EU Regulatory Procedure for Ready-to-Use Propofol Product
BioQ Pharma Incorporated (“the Company”), a specialty pharmaceutical company focused on developing and commercializing ready-to-use infusible pharmaceuticals, today announced the positive closure of a European regulatory procedure for its propofol product. The Company’s ready-to-use infusion pharmaceutical includes the propofol drug product and delivery system in a single-use ...
By BioQ Pharma
-
BioQ Pharma Announces Marijn Dekkers as New Strategic Advisor to the Company
BioQ Pharma Incorporated (“the Company”), a specialty pharmaceutical company, today announced that Dr. Marijn Dekkers has become a strategic advisor to the Company. Concurrent, with his advisory role, Dr. Dekkers also made an investment in BioQ Pharma through his advisory and investment vehicle Novalis LifeScience LLC. Dr. Dekkers is currently the Chairman of Unilever and the Founder ...
By BioQ Pharma
-
Marijn Dekkers to Join BioQ Pharma’s Board of Directors
BioQ Pharma Incorporated (“the Company”), a specialty pharmaceutical company, today announced that Dr. Marijn Dekkers has agreed to join the Company’s board of directors. Dr. Dekkers is founder and chairman of Novalis LifeSciences, an investment and advisory firm for the life science industry. He served as CEO of Bayer AG, a global life sciences company, from 2010 to 2016 and ...
By BioQ Pharma
-
BioQ Pharma Receives CE Mark for Third Infusion System
BioQ Pharma Incorporated (“the Company”), a specialty pharmaceutical company, today announced receipt of CE mark approval in the European Union for its OneDose ReadyfusOR Gen2, single-use medication dispenser. The OneDose ReadyfusOR Gen2 is the second generation of the Company’s original OneDose ReadyfusOR infusion system and was developed to further improve patient convenience. ...
By BioQ Pharma
-
back to overview Help for clinics, nursing services and medical practices
sfm medical devices in Wächtersbach wants to support the supply of protective masks (MNS masks and FFP2) sfm medical devices, a medium-sized med-tech company based in Wächtersbach, sees itself as responsible for providing support in the currently tense procurement situation for protective masks. At the end of March, a concept was developed in collaboration with the company's Medical ...
-
ASTM F1980 - 07(2011) standard guide for accelerated aging of sterile barrier systems for medical devices
The loss of sterile barrier system integrity may occur as a result of physical properties of the materials and adhesive or cohesive bonds degrading over time and by subsequent dynamic events during shipping and handling. ISO 11607–1:2006, clause 6, states that “the packaging system shall provide physical protection and maintain integrity of the sterile barrier system. The sterile ...
-
Water for Sterilizing Medical Devices (AAMI ST108)
Water for sterilization has a new requirement and standard. This applies to surgical tools and instruments, and is useful to feed steam sterilizers and autoclaves.Medical Surgical Devices Require Steriliza New Standard AAMI calls the new standard for water for sterilizing medical devices “Water for the Processing of Reusable Medical Devices”. This is technically AAMI ST108. The ...
-
ASTM F2038 - 00(2011) Standard Guide for Silicone Elastomers, Gels, and Foams Used in Medical Applications Part I—Formulations and Uncured Materials
4.1 This guide is intended to provide guidance for the specification and selection of silicone materials for medical device applications. Silicone manufacturers supplying materials to the medical device industry should readily provide information regarding non-proprietary product formulation to their customers either directly, or ...
-
Industry experts combine to create safer intravenous delivery
The Italian Biochemical Institute (IBI) “Lrenzini”, Comecer, and Particle Measuring Systems (PMS) recently partnered to leverage and combine the expertise of each entity to design a new drug delivery system and a filling line to safely and effectively manufacture it. A Quality Risk Management (QRM) approach was used as the basis to meet the distinctive needs of the aseptic filling ...
-
BioQ Pharma Receives Australian Regulatory Approval for Propofol Product - Propofusor 1%
BioQ Pharma Incorporated (“the Company”), a specialty pharmaceutical company, today announced that the Australian Therapeutic Goods Administration (TGA) has approved the Company’s Propofusor product containing 1% propofol in a single-use dispensing system. Uses of the Propofusor include the induction and maintenance of general anesthesia, sedation of mechanically ventilated ...
By BioQ Pharma
-
Glutaraldehyde in the hospital environment
Glutaraldehyde isfound in the hospital environment at higher concentrations than those to which the general population is exposed. It's possible adverse health effects are therefore very important to those working in certain parts of hospitals and to patients whose health status may be compromised. The compound is an irritant and can cause sensitisation Glutaraldehyde is a colourless liquid ...
Need help finding the right suppliers? Try XPRT Sourcing. Let the XPRTs do the work for you