Lift threads are considered health products and need registration at Anvisa so that they can be marketed and used by health professionals.
This type of product is used as an aesthetic purpose to combat aging, being an ally in the correction of sagging and stimulating collagen in areas of the body, usually in the face where it is inserted through lift threads.
In this blog post, you will learn more about the lift threads and how registration is done at Anvisa so that it can be marketed.
What are the lift threads?
The lift threads are filaments with small cones that, through a process of fixation between the skin and the skin tissue, instantly make the lifting process in the desired area.
The purpose of the facelift is to soften the skin’s flabbiness, and this procedure is widely used to soften easy aging.
We are in an era in which the advancement of aesthetic methods, the most demanding beauty standard, makes more and more people look for procedures to combat sagging and delay old age.
The lift threads are made up of substances that aim to stimulate the production of collagen that also delay aging and that is why this procedure is in high demand.
Considered an invasive aesthetic process, it is necessary that the professional doctor has quality, safe products, tested by Anvisa, in order to ensure the health and safety of the patient.
The procedure is recommended for people who have some degree of flaccidity or in a preventive manner in order to soften the signs of flaccidity in order to promote a more youthful-looking effect.
Do the lift threads need registration at Anvisa?
Plastic surgeries are considered invasive procedures, and therefore, the safety of the products used must be taken into account.
The lift threads are placed on the patient’s face through small holes, in a procedure that can be performed in the doctor’s office with local anesthesia, considering this a simple and quick aesthetic procedure to be performed. However, every procedure has a risk and the professional must pay attention to this to ensure patient safety.
As we have already said, since it is an invasive treatment, the lift threads are classified as risk health products III, according to Anvisa‘s classification. Thus, it is necessary to follow all the procedures of the process, such as gathering information about the manufacturer, the product, tests, evaluations made by technicians, among others.
It is important that the manufacturer is attentive to the regularization procedures of the company with the GMP certification and the product, since only after registration approved by Anvisa is commercialization done.
How to evaluate the safety of the lift threads?
Lift threads are products that can bring risk to the patient if they are not registered by Anvisa.
Registration is the process that indicates whether the product complies with all safety standards, tests and evaluations of the regulatory body.
Anvisa aims to arrive at whether the product can be consumed safely without risks to the patient. Therefore, it is essential that the product is registered and only after approved by Anvisa it can be marketed.
How to register lift threads at Anvisa?
Risk III health products are products considered by the regulator to be at greatest risk to the patient. In this case, the lift threads are inserted into the patient’s skin and therefore need to offer greater security.
Therefore, products like this require greater bureaucracy and greater requirements for approval by Anvisa.
Licempre, a company specialized in regulatory products, assists in an agile and safe way in the whole process so that you have less bureaucracy and greater security in the approval of your registration.