Taiwan FDA registration e097104fd36c534fac7c22b82b609784
“ENDO-FLEX”Endoscopic Ultrasound Aspiration Needle
TW: “福萊克斯”內視鏡超音波抽吸針
Taiwan·Risk Class 2·MD·ENDO-FLEX GmbH·Registered Feb 18, 2017 – Feb 18, 2022ExpiredRegistration details
- Analysis ID
- e097104fd36c534fac7c22b82b609784
- License Form
- Ministry of Health Medical Device Import No. 029448
- Customs Code
- DHA05602944802
Company information
- Manufacturer
- ENDO-FLEX GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 18, 2017
- Expiry Date
- Feb 18, 2022
About this record
Access comprehensive regulatory information for “ENDO-FLEX”Endoscopic Ultrasound Aspiration Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e097104fd36c534fac7c22b82b609784 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 DatabasePowered by Pure Global AI89,000+ Devices