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"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.

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3fd0f05a23cfdce3e9599e1dca250bce
Registration Details
Taiwan FDA Registration: 3fd0f05a23cfdce3e9599e1dca250bce
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Device Details

"Shirley" cystoscopy
TW: โ€œ้›ช่މโ€่†€่ƒฑ้ก
Risk Class 2
Cancelled

Registration Details

3fd0f05a23cfdce3e9599e1dca250bce

DHA00601882209

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

Apr 24, 2008

Apr 24, 2013

Jun 11, 2015

Cancellation Information

Logged out

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