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Duodenoscopy - Taiwan Registration 5d9e2fdb5e952afc831f39694a9ecbbd

Access comprehensive regulatory information for Duodenoscopy in Taiwan's medical device market through Pure Global AI's free database. is registered under number 5d9e2fdb5e952afc831f39694a9ecbbd and manufactured by AMERICAN CYSTOSCOPE MAKERS INC.. The authorized representative in Taiwan is YUNG HUNG HONG.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including AIZU OLYMPUS CO., LTD, FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, and 5 recent registrations in the same category. 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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5d9e2fdb5e952afc831f39694a9ecbbd
Registration Details
Taiwan FDA Registration: 5d9e2fdb5e952afc831f39694a9ecbbd
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Device Details

Duodenoscopy
TW: ๅไบŒๆŒ‡่…ธ็ชบ้ก
Cancelled

Registration Details

5d9e2fdb5e952afc831f39694a9ecbbd

DHA00600197302

Company Information

United States

Product Details

0919 Duodenoscopy

import

Dates and Status

Apr 14, 1982

Apr 14, 1987

Oct 27, 1986

Cancellation Information

Logged out

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