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

PRP tubes | Vi PRP-PRO | with Anticoagulant PU 10 pieces

The VI PRP-PRO glass tube offers a modern solution for producing platelet-rich plasma (PRP) and ensures additional stability and reliability in treatments with a wall thickness of 2.4 mm. Developed with innovative technology and EC-certified (0425-MED-004180-00), it guarantees the highest level of safety and efficiency.

Key Features:

  • Certified quality: Medical device of risk class IIa.
  • Innovative separator gel: Biocompatible and thixotropic for precise separation.
  • Optimized PRP extraction: Produces 4–4.5 ml of PRP per tube.
  • Order No. (PZN): 18354916 New number: 19272445
100101
immediately available
€131.00
incl. tax, plus shipping Shipping excluded | Delivery time 2 - 3 days within Germany* | Abroad may vary

Graduated price - order from quantity Unit price You save in total
3 €130.00 €3.00
5 €129.00 €10.00
8 €126.95 €32.40
 
CE-marked PRP tube for medical professionals

Vi PRP-PRO PRP tubes: 9 ml borosilicate glass with sodium citrate and separation gel

Vi PRP-PRO is a sterile, CE-marked class IIa medical device for the professional preparation of platelet-rich plasma (PRP). The vacuum tube is made of borosilicate glass and contains 0.8 ml sodium citrate as an anticoagulant plus a thixotropic separation gel. One sales unit contains 10 tubes. The standard centrifugation protocol is 1200 × g for 7 minutes.

CE 0425CE marking of the medical device
Class IIaClassification under Directive 93/42/EEC
approx. 9 mlintended vacuum blood draw volume
1200 × gstandard RCF at 7 minutes
10 tubessterile tubes per sales unit

Certification and regulatory status

For practices, clinics and medical procurement teams, regulatory documentation is a central part of product selection. Vi PRP-PRO is CE-marked as a class IIa medical device under Directive 93/42/EEC and is covered by EC certificate 0425-MED-004180-00.

CE marking CE 0425

Identification number 0425 belongs to the notified body ICIM S.p.A., which issued the underlying EC certificate.

Risk class Class IIa medical device

The current classification is based on the European Medical Devices Directive 93/42/EEC.

EC certificate 0425-MED-004180-00

The PRP-PRO commercial variant was added to the certificate scope by an ICIM confirmation dated 22 November 2023.

MDR transition Conformity assessment initiated

The formal MDR application and the written agreement with notified body PCBC, identification number 1434, have been confirmed.

Regulatory status: Vi PRP-PRO is currently supplied as a CE-marked class IIa legacy device under the applicable MDR transitional provisions. The MDR conformity assessment has been initiated and the required written agreement with the notified body has been concluded. The confirmation states a transition period until 31 December 2028, subject to continued fulfilment of the legal conditions.

Request documents for procurement and quality management
Vi PRP-PRO packaging for borosilicate glass PRP tubes with CE 0425 and class IIa marking
Vi PRP-PRO PRP tubes Product packaging of the CE-marked PRP tubes for medical professionals.

Which PRP workflows is Vi PRP-PRO intended for?

Vi PRP-PRO is designed for a professional PRP workflow using sodium citrate and a physical gel barrier. Selection should be based on the intended purpose, instructions for use, available centrifuge and the internal preparation protocol.

Suitable for professional users who

  • need a borosilicate glass PRP tube designed for approximately 9 ml blood draw,
  • use sodium citrate as an anticoagulant and a thixotropic separation gel,
  • work with the defined standard value of 1200 × g for 7 minutes,
  • plan for a possible PRP yield of approximately 4–4.5 ml per tube,
  • prefer a sales unit containing 10 sterile tubes.

Clear distinction from other tube systems

  • Vi PRP-PRO is not a classic PRF tube without anticoagulant.
  • Vi PRP-PRO is not a diagnostic-only laboratory tube.
  • Vi PRP-PRO does not contain melatonin.
  • Tubes with and without anticoagulant or separation gel should not be interchanged without verification.

Technical data for Vi PRP-PRO PRP tubes

The following product profile combines the key information for purchasing, documentation and comparison with the existing clinical or laboratory workflow.

Product name
Vi PRP-PRO PRP tubes with anticoagulant and separation gel
Item number
100101
Manufacturer
D-BIOTECH S.R.L.S., Catania, Italy
Pack contents
10 sterile tubes
Vacuum / blood draw
Designed for approximately 9 ml blood draw per tube
Material
Borosilicate glass, wall thickness 2.4 mm
Anticoagulant
0.8 ml sodium citrate
Separation component
Biocompatible, thixotropic separation gel
Melatonin
Not included
Possible PRP yield
Approximately 4–4.5 ml per tube; the actual volume depends on the starting material and preparation process
Standard centrifugation
1200 × g for 7 minutes
CE marking
CE 0425
Risk class
Class IIa under Directive 93/42/EEC
EC certificate
0425-MED-004180-00
MDR status
Conformity assessment initiated; supplied under the applicable MDR transitional provisions
Intended users
Qualified medical professionals and professional purchasers
Current PZN
19272445
Previous PZN
18354916 – may still be printed on existing stock packaging
Note on the PZN numbers: The current PZN is 19272445. Depending on the available batch, the previous PZN 18354916 may still appear on the packaging. Both numbers refer to Vi PRP-PRO; the product name and item number 100101 should also be checked.
1200 × gfor 7 minutes

Standard centrifugation: 1200 × g for 7 minutes

For Vi PRP-PRO, the technical standard value is a relative centrifugal force of 1200 × g with a runtime of 7 minutes. The required speed in rpm depends on the maximum rotor radius of the centrifuge used.

The calculation requires the distance from the axis of rotation to the bottom of the inserted tube in its operating position. An rpm value must therefore not be transferred unchecked from one centrifuge model to another.

Calculate RCF/RPM for the centrifuge View suitable centrifuges

Reference values for selected centrifuges

For Vi PRP-PRO, the target value is 1200 × g with a runtime of 7 minutes. The following speeds are rounded reference values for selected devices.

Hettich EBA 200 / EBA 200 MD

approx. 3500 rpm

Reference value for 1200 × g

Hettich EBA 270

approx. 2900 rpm

Reference value for 1200 × g

SERVOspin Evolve

approx. 3400 rpm

Reference value for 1200 × g

Important: These values must not be treated as universal device settings. The actual rotor radius, rotor, adapter, tube position and the instructions for use of both tube and centrifuge remain decisive. If the configuration differs, the required speed must be recalculated.

Calculate RCF and RPM for your centrifuge

Vi PRP-PRO in the professional preparation workflow

The following overview is provided for technical orientation. The current instructions for use, approvals for the centrifuge used and the work instructions of the responsible medical facility remain binding.

1. Intended blood draw

The vacuum is designed for a blood draw of approximately 9 ml. The tube already contains 0.8 ml sodium citrate and the thixotropic separation gel.

2. Centrifugation by RCF

The standard value is 1200 × g for 7 minutes. Rotor, adapter and tubes must be loaded symmetrically and balanced according to the device instructions.

3. Separation of blood fractions

During centrifugation, the separation gel supports the physical separation of the fractions. Further withdrawal is performed according to the approved system workflow using suitable sterile accessories.

4. Documentation and compatibility

In addition to RCF and runtime, the centrifuge model, rotor, adapter, batch and accessories used should be documented where required by the internal quality or hygiene management system.

How to compare PRP tubes correctly

A PRP tube should not be selected solely by material or price. Intended purpose, additives, intended blood draw, centrifugation protocol and compatibility with the existing system are decisive. Vi PRP-PRO is clearly defined as a glass tube with sodium citrate and separation gel.

Compare PRP tubesProducts, pack sizes and tube systems for professional users.RCF/RPM calculatorConvert relative centrifugal force and rpm using the actual rotor radius.With or without separation gel?Technical differences between PRP and PRF-related workflows.Glass or plastic?Assess material properties within the complete tube system.

Regular demand for Vi PRP-PRO?

A practice pack containing 40 tubes is also available for clinics with higher consumption. This makes recurring orders and stock planning easier to consolidate.

Practice pack with 40 tubes

International availability through prpmed.de

prpmed.de supplies Vi PRP-PRO to professional customers in numerous European and international markets. Actual availability depends on the destination country, the available shipping route and the applicable import and product regulations.

Available destinations and shipping costs are displayed during checkout. Early demand planning may be useful for larger quantities, recurring orders or distributor enquiries.

Frequently asked questions about Vi PRP-PRO

What is Vi PRP-PRO?

Vi PRP-PRO is a sterile vacuum tube made of borosilicate glass for professional PRP preparation. It is designed for approximately 9 ml blood draw and contains 0.8 ml sodium citrate plus a thixotropic separation gel.

How much PRP can be obtained per tube?

Approximately 4–4.5 ml PRP per tube can be used as an orientation value. The actual volume depends on the starting material and the preparation process used.

Which centrifugation protocol applies to Vi PRP-PRO?

The standard value is 1200 × g for 7 minutes. The required rpm is calculated using the maximum rotor radius of the centrifuge used.

Why does the rpm value differ between centrifuges?

Relative centrifugal force depends on both speed and rotor radius. The same target RCF may therefore require different rpm values in different centrifuges.

Does Vi PRP-PRO contain melatonin?

No. Vi PRP-PRO contains sodium citrate and a thixotropic separation gel, but no melatonin.

Is Vi PRP-PRO a PRF tube?

Vi PRP-PRO is a PRP tube with sodium citrate and separation gel. Classic PRF tubes are often used without anticoagulant and are therefore not equivalent to Vi PRP-PRO.

Why are two PZN numbers listed?

The current PZN is 19272445. Existing stock packaging may still show the previous PZN 18354916, which is why both numbers are stated transparently.

Who is Vi PRP-PRO intended for?

The product is intended for qualified medical professionals and professional purchasers in practices, clinics and medical facilities. Use and preparation must follow the instructions for use and internal requirements.

Is international shipping available?

Shipping is available to numerous countries. Whether a specific delivery can be offered depends on the destination country, shipping route and applicable import and product regulations.

Which CE marking does Vi PRP-PRO carry?

Vi PRP-PRO carries the CE 0425 marking and is classified as a class IIa medical device under Directive 93/42/EEC. The product is covered by EC certificate 0425-MED-004180-00.

What is the current MDR status of Vi PRP-PRO?

Vi PRP-PRO is currently supplied as a CE-marked legacy device under the applicable MDR transitional provisions. A formal MDR application and the written agreement with the responsible notified body have been confirmed.

Professional and regulatory notice: The information on this page describes technical product characteristics and the documented regulatory status and does not replace the current instructions for use, declarations of conformity or certificate documents. Before use, the intended purpose, manufacturer documentation, centrifuge approval, rotor and adapter compatibility and internal work instructions must be checked.
Features
PRP TECHNOLOGY FOR PROFESSIONAL USERS

PRPmed.de – Specialist shop for PRP technology

Carefully selected products for the professional collection, preparation and application of platelet-rich plasma.

Focused specialist range Practical product data Shipping to many countries
PRPmed.de

What is PRP?

PRP stands for platelet-rich plasma. Centrifugation is used to obtain a plasma fraction with an increased platelet concentration from a blood sample. PRP is used and scientifically investigated in a range of medical and aesthetic fields. A qualified practitioner assesses whether an application is appropriate based on the indication and the procedure used.

PRPmed.de

Products for structured PRP workflows

01

PRP and PRF tubes

Different tube systems for defined preparation workflows, with clear information on materials, additives and intended purpose.

02

Centrifuges

Compact devices and coordinated sets for practices and laboratories. RCF, rotor, tube compatibility and manufacturer instructions are key.

03

Needles and accessories

KIPIC® injection needles, blood collection systems, syringes and complementary consumables for professional users.

✓

Clear information instead of broad promises

When selecting products, we look for transparent technical data, a clearly defined intended purpose and sensible component compatibility. Many product pages include information on materials, fill volume, additives, centrifugation and regulatory status. A single product cannot guarantee a medical outcome.

i

Personal support

Our customer service team assists with questions about products, availability and suitable accessories. Medical or therapeutic decisions remain the responsibility of appropriately qualified professionals.

Find the right materials for your workflow

Compare tubes, centrifuges and complementary PRP products directly in the specialist shop.

View PRP tubes View centrifuges Open PRP range

Note: PRPmed.de does not provide medical advice or treatment recommendations. Product selection, preparation and use must be carried out by qualified professionals in accordance with the intended purpose and instructions for use.

 

GPSR – General Product Safety Regulation

Responsible Economic Operator according to GPSR:

prpmed Funkner e.K.

Siemensstraße 32
35440 Linden

Germany

Phone: +49 6043 9862 817

Email: [email protected]

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