Pure Global

"Flex" esophageal dilator - Taiwan Registration 7be9fb85bf73f2a5119b9dffef833d35

Access comprehensive regulatory information for "Flex" esophageal dilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7be9fb85bf73f2a5119b9dffef833d35 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
7be9fb85bf73f2a5119b9dffef833d35
Registration Details
Taiwan FDA Registration: 7be9fb85bf73f2a5119b9dffef833d35
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Flex" esophageal dilator
TW: "็ฆ่Šๅ…‹ๆ–ฏ"้ฃŸ้“ๆ“ดๅผตๅ™จ
Risk Class 2

Registration Details

7be9fb85bf73f2a5119b9dffef833d35

DHA00601772608

Company Information

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

Jan 25, 2007

Jan 25, 2022