Arthrex Drucker Zentrifuge

Arthrex

PRP / laboratory centrifuge

Tabletop centrifuge for PRP (Autologous Conditioned Plasma) preparation

CE Marked medical centrifuge platform for therapeutic / laboratory use in accordance with applicable EU and UK medical device regulations.
Manufactured under an ISO 13485 Compliant quality management system for medical devices (Drucker Diagnostics, in partnership with Arthrex for ACP configuration).
Designed and tested to meet relevant electrical safety and electromagnetic compatibility standards for medical and laboratory equipment.

CE Marked medical centrifuge platform for therapeutic / laboratory use in accordance with applicable EU and UK medical device regulations.
Manufactured under an ISO 13485 Compliant quality management system for medical devices (Drucker Diagnostics, in partnership with Arthrex for ACP configuration).
Designed and tested to meet relevant electrical safety and electromagnetic compatibility standards for medical and laboratory equipment.

Tabletop centrifuge for PRP (Autologous Conditioned Plasma) preparation

Description

The Arthrex Drucker Zentrifuge is a tabletop therapeutic centrifuge (based on the Drucker Horizon 24 Flex platform) supplied for use with the Arthrex ACP (Autologous Conditioned Plasma) double-syringe and ACP Max PRP systems. It is designed to provide consistent, controlled centrifugation of whole blood to prepare low-leukocyte platelet-rich plasma (PRP) / autologous conditioned plasma at the point of care. The unit is a 6-tube horizontal general-purpose centrifuge, optimised via dedicated buckets and spacers for Arthrex ACP double syringes and compatible collection tubes. It features preset programmes recommended by Arthrex for ACP preparation, simple interface, and compact footprint suitable for clinics offering orthobiologic and aesthetic PRP treatments.

Bnefits

Configured specifically for Arthrex ACP and ACP Max PRP systems, ensuring reproducible PRP preparation conditions
Compatible with Arthrex ACP double syringe and standard blood collection tubes via dedicated buckets and spacers
Tabletop, compact design suitable for clinics, aesthetic practices and orthopaedic offices
Horizontal rotor design that promotes consistent separation of plasma and cellular components
Simple, user-friendly interface with fixed programmes / settings recommended by Arthrex for ACP preparation
Reliable centrifugation performance supporting consistent platelet concentration and sample quality
CE-marked medical centrifuge platform from a specialist manufacturer (Drucker Diagnostics)
Single device can support a wide range of PRP and orthobiologic protocols where the Arthrex ACP system is used

Indications

Centrifugation of whole blood to prepare Autologous Conditioned Plasma (ACP) / platelet-rich plasma using the Arthrex ACP double-syringe system
Use with ACP Max PRP system as per Arthrex protocols and accessory kits
General PRP preparation in orthopaedics, sports medicine and regenerative therapies when used with compatible disposables
PRP preparation for aesthetic dermatology and hair restoration procedures in clinics using Arthrex ACP consumables

Composition

Benchtop centrifuge unit with integrated motor and control electronics
6-place horizontal (swing-out) rotor compatible with appropriate buckets for Arthrex ACP double syringes and blood tubes
Steel and high-strength polymer housing with viewing lid and safety interlock
Digital control panel / display (time and speed / RCF, depending on configuration)
Power supply unit for standard mains voltage (region-specific)

Formulation

Non-sterile, reusable electromechanical medical device
6-tube horizontal general-purpose centrifuge (Horizon 24 family) configured for PRP preparation
Designed to operate at PRP-appropriate speeds (e.g. up to ~3200 rpm / ~1900 g for ACP protocols) with fixed or programmable runs
Intended for indoor use in clinical environments on a stable benchtop surface

Packaging

Single Arthrex Drucker centrifuge unit
Supplied with appropriate rotor and buckets for ACP / PRP use (configuration may vary by distributor package)
Power cable and basic accessories as specified in the user manual
Printed instructions for use / user manual
Shipped in protective outer carton with internal foam or moulded inserts to protect the centrifuge in transit

Usage

For professional use only; the Arthrex Drucker Zentrifuge must be operated by trained healthcare staff familiar with Arthrex ACP/PRP protocols and the centrifuge user manual.
Place the centrifuge on a stable, level surface and connect to a suitable mains power supply as specified by the manufacturer.
Install the rotor, buckets and any Arthrex-specific spacers according to the Drucker / Arthrex instructions, ensuring all components are correctly seated and tightened.
Prepare Arthrex ACP double syringes or compatible blood tubes with patient blood according to Arthrex ACP / ACP Max protocols and relevant anticoagulant guidance.
Place syringes or tubes symmetrically in the rotor to ensure proper balance; use counterbalance devices where required.
Close and lock the centrifuge lid; select the recommended programme or set the speed and time according to Arthrex PRP preparation instructions.
Start the run and do not open the lid until the rotor has come to a complete stop and the unit signals that the cycle has ended.
After centrifugation, remove the ACP double syringe or tubes using appropriate aseptic technique and proceed with PRP separation as per Arthrex guidance.
Clean and disinfect the rotor, buckets and centrifuge chamber regularly following the manufacturer’s cleaning instructions and local infection-control policies; do not use corrosive or incompatible cleaning agents.
Perform routine maintenance and safety checks (e.g. rotor inspection, lid lock function) at intervals recommended in the user manual, and arrange service through authorised channels if any abnormalities are detected.

Contraindications

Do not use the centrifuge for any purpose other than centrifugation of blood or compatible fluids in appropriate, closed containers as specified by the manufacturer.
Do not operate the device if the rotor, buckets or internal components are visibly damaged, corroded or out of balance.
Do not use with cracked, overfilled or incompatible tubes / syringes that may break during centrifugation.
Use of the device is contraindicated if local electrical or safety standards cannot be met or if the unit cannot be properly grounded.
Clinical contraindications for PRP treatment (e.g. certain haematologic disorders, anticoagulation, active infection) must be observed even though they relate to the therapy and not the centrifuge hardware.

Adverse Effects

No direct patient adverse effects are expected from correct use of the centrifuge; potential risks relate to device misuse, such as tube breakage, sample loss or aerosol generation if containers fail.
Improper balancing or over-speed operation may cause excessive vibration, noise or mechanical stress, potentially leading to equipment damage or, in extreme cases, mechanical failure.
Failure to follow cleaning and disinfection instructions may increase the risk of environmental contamination in the clinical area.

Storage Conditions

Store and operate the centrifuge in a clean, dry indoor environment at ambient room temperature within the range specified by the manufacturer (typically approximately 10–40°C).
Keep away from direct sunlight, excessive heat sources, and corrosive or flammable vapours.
When not in use for extended periods, switch off the device, unplug from the mains, and keep the lid closed to prevent dust ingress.
Do not store heavy items on top of the centrifuge or subject it to shocks or vibrations that could damage internal components.
Transport the unit only in its original or equivalent protective packaging to avoid mechanical damage.

Duration

Not directly applicable to the device itself. Typical PRP preparation runs for Arthrex ACP systems are short single-spin cycles (on the order of several minutes), as defined in Arthrex protocols; the centrifuge cycle time is set via its control panel according to these instructions.

Onset

Not applicable to the centrifuge as a device. Effective separation of plasma and cellular components is achieved immediately after completion of the centrifugation cycle, after which PRP is ready for clinical use according to the relevant protocol.