"Shirley" cystoscopy - Taiwan Registration 3fd0f05a23cfdce3e9599e1dca250bce
Access comprehensive regulatory information for "Shirley" cystoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fd0f05a23cfdce3e9599e1dca250bce and manufactured by SCHOLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
H Gastroenterology and urology
H.1500 Internal Scope and its accessories
import
Dates and Status
Apr 24, 2008
Apr 24, 2013
Jun 11, 2015
Cancellation Information
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