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"Xuli" cystoscopy - Taiwan Registration 90d4295375ae3e622db59ad02dea748a

Access comprehensive regulatory information for "Xuli" cystoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 90d4295375ae3e622db59ad02dea748a and manufactured by SCHร–LLY FIBEROPTIC GMBH. The authorized representative in Taiwan is ENTMED CO., LTD..

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.

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90d4295375ae3e622db59ad02dea748a
Registration Details
Taiwan FDA Registration: 90d4295375ae3e622db59ad02dea748a
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Device Details

"Xuli" cystoscopy
TW: โ€œๆ—ญ้บ—โ€่†€่ƒฑ้ก
Risk Class 2

Registration Details

90d4295375ae3e622db59ad02dea748a

DHA05603426501

Company Information

Germany

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

Jan 17, 2021

Jan 17, 2026