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"Flex" esophageal balloon dilation catheter - Taiwan Registration 77c1feb5ceedb19778d4adc03a3efcfc

Access comprehensive regulatory information for "Flex" esophageal balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77c1feb5ceedb19778d4adc03a3efcfc and manufactured by ENDO-FLEX GMBH. The authorized representative in Taiwan is SHIUH-CHYNG MEDICAL 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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77c1feb5ceedb19778d4adc03a3efcfc
Registration Details
Taiwan FDA Registration: 77c1feb5ceedb19778d4adc03a3efcfc
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Device Details

"Flex" esophageal balloon dilation catheter
TW: โ€œ็ฆ่Šๅ…‹ๆ–ฏโ€้ฃŸ้“ๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2
Cancelled

Registration Details

77c1feb5ceedb19778d4adc03a3efcfc

DHA00601801901

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.5365 Esophageal extenders

import

Dates and Status

Apr 14, 2007

Apr 14, 2012

Jul 25, 2014

Cancellation Information

Logged out

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