Boston, MA -- (ReleaseWire) -- 02/12/2014 -- Miromatrix Medical Inc. (Miromatrix Medical) is a regenerative medicine developer. The company undertakes development of perfusion decellularization technology. It works on various organs by running a detergent through the blood vessels. The company creates biological replacement organ for the human body such as the liver, heart, lung, kidney and pancreas. Miromatrix Medical develops and produces biomesh from porcine organ tissue for abdominal wall and hernia repair and breast reconstruction. It provides solutions for extracorporeal liver graft, revascularized liver lobe, transplantable liver, and recellularized liver lobe. The company also provides patching solutions, bioengineered patch and cardiac solutions. Miromatrix Medical is headquartered in Eden Prairie, Minnesota, the US.
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This report is a source for data, analysis and actionable intelligence on the Miromatrix Medical Inc. portfolio of pipeline products. The report provides detailed analysis on each pipeline product with information on the indication, the development stage, trial phase, product milestones, pipeline territory, estimated approval date, and estimated launch date.
Each pipeline product is profiled to cover information on product description, function, technology, indication, and application. The report is also supplemented with a detailed company profile and information on clinical trials, wherever applicable.
This report is built using data and information sourced from proprietary databases, primary and secondary research and in-house analysis by GlobalData's team of industry experts.
- Detailed company profile with information on business description, key company facts, major products and services, key competitors, key employees, locations and subsidiaries and recent developments.
- Detailed coverage on all the pipeline products, by equipment type, by therapy area, by development stage, and by trial phase.
- Information on product milestones and pipeline territory for each product, the estimated approval date, and estimated launch date.
- Profile of each pipeline product with additional information on product description, function, technology, indication(s), and application.
- Data on relevant clinical trials and product patent details, wherever applicable.
- Information on clinical trial, wherever applicable, is supplemented with information on trial phase, trial status, trial objective, trial design, target patients, unique physician identifier, primary point, secondary point, acronym, participants inclusion, participants exclusion, interventions, trial results, trial start date, trial end date, study type, trial site, trial funding, age eligibility, and gender eligibility.
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