Taiwan FDA registration 4316e21cb08d82d3a4de17ef7d8d7231
"Nocod" ureteral access catheter sheath
TW: “諾可得”輸尿管通路導管鞘
Taiwan·Risk Class 2·PROMEDTECH;; ROCAMED FRANCE·Registered Jul 13, 2021 – Jul 13, 2026ExpiredRegistration details
- Analysis ID
- 4316e21cb08d82d3a4de17ef7d8d7231
- Customs Code
- DHA05603470503
Company information
- Manufacturer
- PROMEDTECH;; ROCAMED FRANCE
- Manufacturer Country
- Tunisia;;France
- Authorized Representative
- KUAN FWA MED CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 內視鏡及其附件;; H.5130 泌尿導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Jul 13, 2021
- Expiry Date
- Jul 13, 2026
About this record
Access comprehensive regulatory information for "Nocod" ureteral access catheter sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4316e21cb08d82d3a4de17ef7d8d7231 and manufactured by PROMEDTECH;; ROCAMED FRANCE. The authorized representative in Taiwan is KUAN FWA MED CO., LTD..
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