Taiwan FDA registration e80483f8940b39990af727694cba4070
“Lake Region”Introduction/Drainage Catheter and Accessories (Non-Sterile)
TW: “雷科理均”導入/引流導管及其附件(未滅菌)
Registration details
- Analysis ID
- e80483f8940b39990af727694cba4070
- License Form
- Ministry of Health Medical Device Import No. 014171
- Customs Code
- DHA09401417100
Company information
- Manufacturer
- LAKE REGION MEDICAL LTD.
- Manufacturer Country
- Ireland
- Authorized Representative
- JI SHENG MEDICAL COMPANY LIMITED
Product details
- Intended Use
- Limited to the scope of Grade 1 identification of "Introduction/Drainage Catheters and Their Accessories (I.4200)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4200 Introduction/drainage catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 23, 2014
- Expiry Date
- May 23, 2024
About this record
Access comprehensive regulatory information for “Lake Region”Introduction/Drainage Catheter and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e80483f8940b39990af727694cba4070 and manufactured by LAKE REGION MEDICAL LTD.. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.
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