Hello, versatility.

BioAssemblyBot 200 is a versatile powerhouse bioprinter. BAB200 takes three forms: biosafety cabinet ready, enclosed, and enclosed with HEPA filtration. Whether you are using the four-axis arm bioprint, pick up well plates, or pipette material, BAB200 is built for the modern lab.

Overview

Three of a kind.

BioAssemblyBot 200 can transform into three unique forms to meet your needs. BAB200 is perfect for working under a biosafety cabinet, enclosed is perfect for the lab benchtop and enclosed with HEPA filtration is perfect for biology where air quality must be maintained.

A tool for every need.

BAB200 swaps "hands" allowing users to 3D bioprint with temperature control, move well plates, and pipette with up to five different BioAssemblyBot Hands in one run.

Explore BioAssemblyBot Hands

Advantages

Collaborate with others.

Supercharge your collaboration. Expand collaborative opportunities with new people and equipment that integrates directly into your existing lab ecosystem.

Solve problems, faster.

Prove your hypothesis in fast, efficient ways with automation. Get back to "doing the science" that you love by eliminating time consuming repetitive tasks.

Develop curative solutions.

Focus on deeply personalized medicine by implementing curative solutions and not just symptom management cost effective and time efficient solutions.

Scale up R&D.

Enable product innovation with quick testing and simplified complex manufacturing processes. Cause a positive impact on your department's bottom line.

Design with TSIM.

Create complex, biomimetic objects from medical imaging with easy-to-use point & click 3D software.

Explore TSIM

Automate with BioApps.

Drag & drop and rearrange your experimental protocol or use one from the community.

Explore BioApps

Load in Materials & Go.

Add in your biomaterials and press Go. BAB will do the rest and let you know when she's done.

Explore Materials

Process

Gallery

BioAssemblyBot 200 Key Features & Specifications:

Tech Specs

Compare with other BioBots

Removable Enclosure

HEPA Filtration System

4-Axis Robotic Arm

Use up to 5 compatible BioAssemblyBot Hands

Adaptive Tip Detection

Temperature Controlled Print Stage

UL cGMP Certified

Required electrical cabinet and touch screen interface not shown.

4-axis

Robotic Arm

BioAssemblyBot Hands in a single run

Detached touch screen controls

HEPA Filtration Optional

Biosafety Cabinet

Compatible without enclosure

Compatible

Build Volume

11 in (l) x 7 in (w) x 2.75 in (h)

27.9 cm (l) x 17.8 cm (w) x 6.9 cm (h)

3D Printing Technology

Pneumatic or Mechanical Dispense

BioAssemblyBot Hands Compatibility

Works with most tools

HEPA Specifications

HEPA Filtration Optional

Biosafety Cabinet Compatibility

Works with most (w/o enclosure)

Air Flow Requirements

100psi 1cfm

Base

Benchtop or Biosafety Cabinet

Temperature Controls

Stage: 10 to 60 C

3D Syringe | Hot: Up to 150 C

3D Syringe | Cold: Down to -4 C

Connections

Power Supply Input

RJ45 CAT-5

Pneumatic Air Fitting

Electrical Panel

External

Electrical Requirements

Bioprinter:

120V 60 Hz Single Phase @ 15 Amp Isolated Receptacle (NEMA 5-15R)

External Electrical Panel:

120V 60 Hz Single Phase @ 15 Amp Isolated Receptacle (NEMA 5-15R)

Dimensions & Weight

Bioprinter with HEPA filtration:

36.4 in (w) x 26.3 in (d) x 44.5 in (h)

92.46 cm (w) x 66.8 cm (d) x 113.03 cm (h)

175 lbs

79.38 kg

Bioprinter with enclosure:

36.4 in (w) x 26.3 in (d) x 31.4 in (h)

92.46 cm (w) x 66.8 cm (d) x 79.75 cm (h)

140 lbs

63.5 kg

Bioprinter without enclosure:

33.5 in (w) x 24.5 in (d) x 31.1 in (h)

85.09 cm (w) x 62.2 cm (d) x 78.9 cm (h)

120 lbs

54.43 kg

External Electrical Panel:

24 in (w) x 29 in (d) x 23 in (h)

60.96 cm (w) x 73.66 cm (d) x 58.42 cm (h)

Ready to meet BAB200?

Book a demo or get a quote, she can't wait to meet you:

Quote

The Advanced Solutions Louisville, KY facility has been audited by UL Registrar LLC and meets GMP requirements listed in RCP, NBCP, or Pharmaceutical Certification Schemes which is uniquely accredited by the American National Standard Institute (ANSI) developed in accordance with applicable sections of the FDA’s code of federal regulations.