Pure Global

"Flex" endoscope accessory (sterilization) - Taiwan Registration 74853f37bb320441c013790bc0dc4042

Access comprehensive regulatory information for "Flex" endoscope accessory (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 74853f37bb320441c013790bc0dc4042 and manufactured by ENDO-FLEX GmbH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
74853f37bb320441c013790bc0dc4042
Registration Details
Taiwan FDA Registration: 74853f37bb320441c013790bc0dc4042
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Flex" endoscope accessory (sterilization)
TW: "็ฆ่Šๅ…‹ๆ–ฏ" ๅ…ง่ฆ–้ก้™„ไปถ (ๆป…่Œ)
Risk Class 1

Registration Details

74853f37bb320441c013790bc0dc4042

DHA09401555102

Company Information

Product Details

Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Aug 04, 2015

Aug 04, 2025