It is very important to ensure safe and efficient supply of medical gas throughout the medical facility. This is because medical gases like ocygen, nitrogen, nitrous oxide, and helium have to be supplied at a particular pressure and temperature. If not supplied properly, these medical gases can pose a serious safety risk as well. Zeibaq for more than 10 years has been the most trusted and affordable supplier and manufacturer of medical gas systems across Saudi Arabia.
How Can We Help
At Zeibaq, we supply and install complete medical gas pipeline systems that adhere to the international safety and quality standards. Starting right from installing the gas outlet to services for the plant room, we offer everything.
Our medical gas projects include supply & installation of the following:
Your Safety Is Important For Us
Client safety is the top-most priority for Zeibaq. When our experts design a medical gas system, they ensure safety at every step. From using high quality material to following all safety and quality standards, Zeibaq promises best quality medical gas systems. All our products come with certification. Contact us to know more.
Choose The Right Services
If you are looking for services for medical gas systems then Zeibaq is the right choice for you. All you need to do is get in touch with us and we will take care of the rest. You can reach out to us via call, e-mail or simply fill a form available on our website. Our team will carefully study the details shared by you and plan & offer most appropriate solutions for your business.
What is a medical device cleanroom?
A medical device cleanroom is a space where medical devices - both implantable or for external use are manufactured. At times, it also acts as a cleanroom for supplies at some medical device companies.
Who regulates medical device cleanrooms?
Medical devices cleanrooms should adhere to FDA’s Good Manufacturing Practice (GMP).
What type of cleanroom is a medical device cleanroom?
Depending on the criticality of the product, whether it is implantable or sterile, the medical device cleanroom classification can range from ISO-5 to ISO-8.
Do medical devices cleanrooms have air conditioning?
Yes, GMP requires a controlled environment. Usually, there is some kind of medical or medical device manufacturing specification for allowable temperature and humidity that can impact manufacturing of nutraceuticals.
How is a cleanroom different from a conventional lab environment?
A lab may look similar to a cleanroom but there is a difference between both. Cleanrooms are areas that are equipped with ceiling-mounted filtration systems that help remove pollutants from air.
What safety standards a cleanroom should comply with?
All nutraceutical cleanrooms must obey FDA’s Good Manufacturing practices. It should also adhere to ISO 14644-1 standard for air cleanliness as well.
What ISO class is needed for nutraceutical manufacturing?
In most cases, nutraceutical applications need ISO 7 or ISO 8 cleanroom classifications. However, particular needs are based on the process and product sensitivity.
