Table of Contents
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Project Summary
A newborn baby who has been born premature or with an illness will be kept in the Neonatal Intensive Care Unit, NICU, in a hospital. In order for these infants to grow and develop properly, they need to receive clean, uninfected milk from their mothers who are forced to use a breast pump. Breast pumps allow for mothers to still feed their babies and produce milk until they are able to feed directly from the nipple. However, feeding a baby who is in the NICU is not an easy task with the limited space and necessity of a clean pump at all times. Every time a mother pumps milk, she must effectively clean all parts of the pump that touched milk with hot soapy water. This process takes time away from being with their child and can be difficult in small NICU rooms. Currently there are no systems that clean every part of a breast pump without needing other resources such as a microwave.The goals of this project are to create a system that can safely, efficiently, and effectively clean breast pump parts with the constraints found in a NICU room. The ideal system will be able to clean the parts in a fraction of the time it takes to clean them by hand as well as sterilize them and be easy to use. The expected end result will be an automated cleaning system that will clean breast pump parts given the space and resources of a typical NICU room. The design will also follow the guidelines provided by the CDC, FDA and ISO to ensure safety and ability to use the system in a hospital.
Use Cases
Project Goals and Key Deliverables
- Create an automated cleaning & sterilization system for breast pumps.
- Safe
- Cost Effective
- Easy to Use
- Reliable
Customer Interviews
Date | Person | Questions | Notes |
---|---|---|---|
January 25, 2018 | Dr. Casey Rosen-Carole | Session 1 | |
January 29, 2018 | A Mother | Session 1 | |
January 30, 2018 | Mothers | Session 1 |
Customer Requirements (Needs)
- In addition to a snapshot, include a link to the live document here
Engineering Requirements (Metrics & Specifications)
- References:
https://edge.rit.edu/edge/PTemplate/public/Establish%20Engineering%20Requirements
- Considering the purpose, the team should anticipate potential failure modes associated with construction and use of this document.
Constraints
- Follow CDC, FDA and ISO guidelines
- Testing
- Timing
- Safety Requirements
House of Quality
Live document located here
Risk Management
Design Review Materials
Plans for next phase
Systems Design (Starts 2/6)- Functional analysis
- Concept Generation
- Engineering Analysis
- Experimentation, teardown, analysis
- First order modeling, analysis, and simulation
February 27th SDR (System Design Review)
- Detailed Design & Component Selection (Starts 3/6)
- Detailed Design
- End state deliverables → Requirements flow-down to subsystems
- POC (Proof-of-concept)
- Analysis, simulation, prototyping
April 24th Final DDR (Detailed Design Review)
Individual Plans:
- Angelo's 3-Week plan
- Kyla's 3-Week plan
- Christopher's 3-Week plan
- Yohance's 3-Week plan
- Jake's 3-Week plan
- Meg's 3-Week plan
- Rachel's 3-Week plan
Home | Planning & Execution | Imagine RIT
Problem Definition | Systems Design | Preliminary Detailed Design | Detailed Design
Build & Test Prep | Subsystem Build & Test | Integrated System Build & Test | Customer Handoff & Final Project Documentation