PRP tubes | Vi PRP-Pro | PU 10 pcs.
PRP tubes | Vi PRP-Pro | PU 10 pcs.

PRP tubes | Vi PRP-Pro | PU 10 pcs.

Vi PRP-Pro PRP tubes allow you to easily and efficiently obtain and process platelet-rich plasma (PRP) from patients' blood. These tubes are CE-marked and comply with numerous ISO certifications.

Order No. (PZN): 18354916

Manufacturer article number: 100100

EAN number: 4170000035626

PU 10 piece



immediately available
incl. tax, plus shipping | Delivery time 2 - 3 days within Germany* | Abroad may vary
0.27 kg

Graduated price - order from quantity Unit price You save in total
2 €107.58 €1.96
3 €106.51 €6.15

PRP-PRO tubes, the pinnacle of plasma therapy

Safe and fast! The simplest method for obtaining high-purity and autologous plasma!


With the PRP-PRO, you can harness the power of your body to take healing processes to a new level. It is no longer a secret that the best therapies are those that work with our body's natural mechanisms. PRP-PRO offers just that - an advanced solution for the preparation of autologous plasma rich in platelets that supports and accelerates your healing.

VI - Density Life Platelets PRP Tubes

VI PRP-PRO is a revolutionary product used for the production of platelet-rich plasma (PRP). It consists of special tubes marked with a red cap and anticoagulant. Each tube is designed to hold approximately 9 ml of blood and has a pre-calibrated vacuum that is used to prepare the blood sample. The tubes also contain a separating gel made from an inert polymer that helps to separate the platelet-enriched serum from the red blood cells.

Why PRP-PRO PRP tubes?

Why PRP-PRO PRP tubes?

Trustworthiness through certification: With a CE certificate no. 004180-00 issued by ICIM Spa, an organization with the identification number 0425, PRP-PRO offers the assurance that it complies with all essential requirements of Directive 93/42/CEE and subsequent amendments.

Quality assured: Manufactured to the highest quality standards, compliant with UNI EN ISO 9001 and 13485.

Simple and efficient: Using the latest technology, PRP-PRO enables easy preparation of platelet-rich plasma. This means less time in the treatment room and more time for what really matters in life.

Class IIa medical device: Classified under Class IIa according to Rule 3 of Annex IX of the cited directive, PRP-PRO represents a high level of safety and efficiency.

Why PRP-PRO PRP tubes?

Innovation: The latest variants such as PRP-PRO are known for their revolutionary efficiency and ease of use.

Accessibility: With approval for marketing by the Italian authority, you can be sure that you are getting a product that not only meets the highest standards, but is also easily accessible.

Responsibility: PRPMED stands fully behind its product, with a declaration of sole responsibility for compliance with all relevant regulations and standards.

The PRP-PRO advantage - quality and safety

CE certification: With CE Declaration of Conformity No. 004180-00, validated by ICIM Spa (Notified Body No. 0425), PRP-PRO is tested according to the strictest European standards.

Quality standards: Manufactured according to UNI EN ISO 9001 and 13485, PRP-PRO is committed to the highest quality standards and corporate responsibility.

Efficiency: PRP-PRO enables quick and easy preparation of autologous platelet-rich plasma, which shortens treatment time and improves quality of life.

Classification: As a class IIa medical device, PRP-PRO guarantees a high level of safety and performance for users and patients.

VI PRP-PRO PRP tubes are the latest and most advanced product for the production of platelet-rich plasma (PRP). They are made from high quality materials and are free from micronized silicone, which could affect the quality of the final PRP product.

Each tube has a capacity of 9 ml and can produce approximately 4-4.5 ml of PRP. PRP tubes are intended for use with autologous blood products and can be used to administer localized high concentrations of growth factors to help repair tissue and strengthen hair roots.

They are available in 9 ml vacuum capacity and must be used by specially trained medical personnel under medical supervision.

Fields of application


Reconstruction of the lower jaw, dental implants, tonal and oropharyngeal fissures;

Ear, nose and throat medicine

Neck and head surgery, facial or nasal fractures;

Lesions of the dental alveoli; breast augmentation; reconstruction of the lower jaw; bone graft; oronasal fistula; lip repair; rhinoplasty and septal rhinoplasty; facial fractures


Skin flaps, muscle-skin reconstructions, mammoplasty; face and neck lift; musculocutaneous flaps and reconstruction; chronic ulcers; breast reconstruction and mammoplasty; craniofacial reconstruction; adjunct for laser facial treatments


Pseudoarthrosis, osteosynthesis, bone implants, titanium prosthesis implants


Vertebral reconstruction; burr holes and craniectomy; cerebrospinal fluid loss

Vascular and cardiac surgery

Sternal repair; arterial bypass; arterial reconstruction; broncho-pleural fistula


Corneal ulcers and wounds; repair of macular lesions (with hyperconcentrated platelets).


Regeneration of the hair roots


are specialized areas in which ulcers or acute or chronic ruptures, primary or secondary, could find therapeutic support in the use of platelet gel.

Precautionary measures

The medical device may only be used by experienced personnel and only under certain conditions.

Use the PRP with particular caution in the following cases:

  • acute or chronic infections at the surgical site;
  • uncontrolled metabolic diseases such as diabetes, osteomalacia, thyroid dysfunction, severe kidney or liver disease;
  • Long-term therapy with cortisone;
  • Autoimmune diseases;
  • Radiotherapy.

Patients with congenital or acquired functional platelet defects may release fewer growth factors.

In thrombocytopenia, it is very difficult to obtain a platelet-rich concentrate for clinical use. The platelet gel is reabsorbed within a few days. No toxicity phenomenon has been described in tissues treated with gel.

Normal monitoring procedures or prophylaxis against infectious complications should be used. Platelet-derived growth factors induce cell proliferation.

The use of platelet gel is contraindicated in suspected malignant degenerative lesions. To ensure tissue regeneration, the PRP must only be introduced into vital tissue and in direct contact with the tissue (if necessary, by applying microtints to the surface of the tissue).

By following these instructions for use, a PRP with a platelet concentration 4-5 times higher than the original blood sample (1 x 106 platelets / microliter ± 20%) can be produced with this medical device. Growth factors and chemotactic mediators from platelets are mainly released passively (i.e. without platelet activation). Therefore, platelet gel can be prepared from the blood of patients taking oral anticoagulants, heparin, calcium heparin, platelet aggregation inhibitors and cyclooxygenase inhibitors.

Part of the release of growth factors may depend on the activation state of the platelets. It is therefore advisable to wait for a delay in the release of the growth factors

Growth factors if the patient is taking cyclooxygenase inhibitors or anti-adhesion platelets. There are no known interactions with systemic or topical agents. Intended use does not include adding medications to the platelet gel. If platelet gel is used for bone regeneration, the gel can be used with certified animal bone or certified biocompatible materials.

Application protocol

The production of PRP consists of the collection of autologous venous blood (from the patient to be treated), which is then centrifuged and concentrated (method called BUFFY COAT).

After blood collection, centrifugation (rotation/centrifugal force depending on the centrifuge) is performed until three layers are obtained:

  • platelet-poor plasma (platelet-poor plasma PPP)
  • platelet-rich plasma (platelet-rich plasma-PRP)
  • red blood cells

Set the centrifuge to the following parameters:

1200 RCF (g) (For Hettich EBA 200 to 4000 rpm) for 10 minutes for angled or inclined rotor centrifuges.

To determine the relative centrifugal force (RCF), or to calculate the revolutions per minute (RPM), you can use our converters.


VI PRP-PRO PRP tubes is a new generation product manufactured with advanced technology to improve the quality and efficiency of their use. They are all CE marked (93/42/EEC, updated by Directive 2007/47/EEC) and then validated according to numerous ISO certifications such as ISO 9001: 2008, EN ISO 13485: 2012 and EN ISO14971: 2009, ISO 10993 -1: 2009, ISO 10993-3: 2005.

The PRP tubes are sterile primary packaging. Their packaging takes place in a laminar flow environment and is certified as a Class IIa medical device registered with the Ministry of Health under the national registration number with the CND classification.

PRP tubes

Important note:

As the seller, we would like to point out that the injection of products with and without lidocaine should only be carried out by trained and medically qualified personnel in the medical and nursing field.


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