Taiwan FDA registration 5d9e2fdb5e952afc831f39694a9ecbbd

Duodenoscopy

TW: 十二指腸窺鏡
Taiwan flagTaiwan·AMERICAN CYSTOSCOPE MAKERS INC.·Registered Apr 14, 1982 – Apr 14, 1987Cancelled
Registration details
Analysis ID
5d9e2fdb5e952afc831f39694a9ecbbd
Customs Code
DHA00600197302
Company information
Manufacturer Country
United States
Authorized Representative
YUNG HUNG HONG
Product details
Product Type (Level 1)
0919 Duodenoscopy
Import Information
import
Dates and status
Registration Date
Apr 14, 1982
Expiry Date
Apr 14, 1987
Cancellation Date
Oct 27, 1986
Cancellation information
Status
Logged out
Reason
列屬無須查驗登記項目範圍
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About this record

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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