Custom Ultrasonics’ controversial automated endoscope reprocessor receives limited duodenoscope approval — 4 insights

The FDA granted Custom Ultrasonics’ System 83-plus Automated Endoscope Reprocessor approval to reprocess Olympus TJF-Q180V and Pentax ED-3490TK duodenoscopes.

Advertisement

Here’s what you should know:

1. Custom Ultrasonics completed a series of validation tests, confirming System 83 can clean and disinfect these models to a high degree.

2. All centers must follow the instructions in the updated operator’s manual which describes the newly validated process.

3. System 83-plus cannot be used to reprocess Fujifilm duodenoscopes or duodenoscopes with open elevator wire channels.

4. The FDA and Custom Ultrasonics have been embroiled in a dispute since January 2007 over System 83-plus. The automated endoscope reprocessor has been recalled multiple times, and the FDA has been working with Custom Ultrasonics to get the system and the company back in regulatory compliance.

More articles on gastroenterology:
The 2019 diagnosis code changes are here: 6 things to know
Hennepin Healthcare installs 1st automated endoscope reprocessor in the US — 4 insights
15 statistics on GI starting salary

Advertisement

Next Up in GI & Endoscopy

Advertisement

Comments are closed.