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BIOBASE BPA-SD08 Platelet Agitator — 8-Layer, 60 Oscillations/Minute, LCD Speed Display, Universal Voltage

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SKU:
TWH-BPA-SD08
Weight:
72.75 LBS
Availability: 21-30 Days ETA.

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Description

The BIOBASE BPA-SD08 Platelet Agitator is an eight-layer benchtop agitation system designed to provide controlled, continuous horizontal reciprocating motion for platelet-bag handling workflows in blood banks, transfusion departments, hospitals, laboratories, and research facilities.

The system combines a stainless-steel frame, smooth molded trays, LCD operating-speed display, adjustable motor control, and an AC servo motor intended to support quiet, stable operation. Each layer accommodates two 200 mL bags, providing a nominal total capacity of up to sixteen 200 mL bags when all eight layers are used.

What is the BPA-SD08 all about?

The BPA-SD08 uses a left-to-right horizontal oscillation pattern with a 35 mm movement amplitude and a fixed operating frequency of 60 oscillations per minute. Its removable-style molded trays have smooth, burr-free surfaces designed to reduce the risk of physical damage to blood bags during routine agitation.

An integrated LCD screen displays operating speed, while the speed-adjustable drive system and AC servo motor support smooth and comparatively quiet operation. The stainless-steel structural frame provides a durable, easy-to-clean exterior appropriate for controlled laboratory and blood-processing environments.

The unit operates from a universal AC 100–240 V, 50/60 Hz power supply, allowing deployment across a broad range of domestic and international facilities without separate voltage-specific product variants.

Key Features

  • Eight-layer platelet agitation configuration
  • Two 200 mL bag positions per layer
  • Nominal total capacity of sixteen 200 mL bags
  • Horizontal left-and-right reciprocating motion
  • Fixed frequency of 60 oscillations per minute
  • 35 mm oscillation amplitude
  • LCD operating-speed display
  • Adjustable motor control
  • AC servo motor for smooth operation
  • Mold-injected trays with smooth, burr-free surfaces
  • Stainless-steel frame
  • Easy-to-clean exterior surfaces
  • Programmable timer from 0 to 9,999 minutes
  • Universal AC 100–240 V, 50/60 Hz electrical compatibility

Technical Specifications

Specification BPA-SD08
Brand BIOBASE
Model BPA-SD08
Product Type Platelet agitator
Layer Count 8
Capacity per Layer 2 × 200 mL
Nominal Total Capacity 16 × 200 mL bags
Oscillation Frequency 60 oscillations/minute
Oscillation Amplitude 35 mm
Motion Pattern Horizontal left-and-right reciprocating oscillation
Timing Range 0–9,999 minutes
Display LCD operating-speed display
Drive System Speed-adjustable motor with AC servo motor
Frame Material Stainless steel
Power Supply AC 100–240 V, 50/60 Hz
Condition New
Supply Configuration Factory-direct equipment

Manufacturer specifications confirm the eight-layer design, capacity, motion pattern, electrical requirements, dimensions, and listed weights.

Dimensions and Shipping Information

Measurement Metric Approximate U.S. Measurement
Single-Layer Tray Size 400 × 280 × 40 mm 15.75 × 11.02 × 1.57 in
Equipment Size 423 × 330 × 502 mm 16.65 × 12.99 × 19.76 in
Packaged Size 534 × 439 × 650 mm 21.02 × 17.28 × 25.59 in
Net Weight 25 kg 55.12 lb
Gross Shipping Weight 33 kg 72.75 lb

The metric measurements and weights are manufacturer-published specifications; imperial values are rounded conversions.

SKU and MPN Mapping

Field Identifier
Truway Health SKU TWH-BPA-SD08
Manufacturer Part Number BPA-SD08
Brand BIOBASE
Product Family Blood Bank Instruments
Variant Title BPA-SD08 — 8-Layer, 16 × 200 mL Capacity

Intended Applications

  • Hospital blood banks
  • Blood centers and collection facilities
  • Transfusion-medicine departments
  • Clinical laboratories
  • Biomedical research facilities
  • Platelet-processing workflows
  • Medical teaching laboratories
  • Government and institutional procurement

Included Configuration

  • BIOBASE BPA-SD08 main agitator
  • Eight agitation layers
  • Molded blood-bag trays
  • LCD operating interface
  • Universal-voltage electrical system
  • Standard manufacturer packaging
  • Basic operating documentation, subject to the supplied factory package

Operational Note

The published specifications describe the BPA-SD08 as an agitation-only system. No integrated temperature-controlled chamber or platelet incubator is listed. Facilities requiring controlled-temperature platelet storage should use the agitator within a separately qualified environment or select a compatible incubated platelet-storage system. This conclusion is based on the manufacturer’s listed features and technical parameters.

Cleaning and Maintenance Guidance

Disconnect the unit from electrical power before cleaning. Use cleaning agents compatible with stainless steel, molded tray materials, and the facility’s infection-control procedures. Do not immerse the motor, display, controls, or electrical components. Routine users should inspect the trays, drive mechanism, electrical cord, and oscillation performance before operation.

Warranty

The equipment should be supplied with the written manufacturer or distributor warranty stated in the final commercial invoice, purchase agreement, or tender. Unless expressly expanded in writing, warranty coverage should apply only to defects in materials or workmanship under normal intended use. Warranty coverage should exclude consumables, ordinary wear, improper installation, unauthorized repair, misuse, liquid intrusion, incorrect voltage connection, transit damage not reported within the required period, failure to follow operating instructions, and use outside approved environmental conditions. This equipment does not independently establish the safety, suitability, sterility, potency, quality, or clinical usability of any platelet product. The purchaser remains responsible for facility qualification, operating procedures, environmental controls, staff training, maintenance, validation, regulatory compliance, and blood-product handling practices. No claim of FDA clearance, registration, approval, or authorization should be placed on the U.S. product page unless supported by current, model-specific documentation.

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