CG-100
Commercial- Indications
- Colorectal surgery complications, Anastomotic leaks
Company intelligence / Profile preview
The CG‑100 intraluminal bypass device has completed a prospective multi-center trial with positive safety and feasibility results. It received CE marking in the EU (2014) and has completed verification/validation including animal studies. A pivotal IDE-approved randomized trial for rectal cancer patients is enrolling at multiple sites internationally to support US regulatory approval.
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