Taiwan FDA registration 26485413cc5ee5c64e09e8cb24a8e0e6
"joimax" Versicon Introduction/drainage catheter and accessories (Non-Sterile)
TW: "脊美適" 維思康 導入/引流導管及其附件 (未滅菌)
Registration details
- Analysis ID
- 26485413cc5ee5c64e09e8cb24a8e0e6
- License Form
- Ministry of Health Medical Device Import No. 016663
- Customs Code
- DHA09401666305
Company information
- Manufacturer
- JOIMAX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- K&C MEDICAL CO., LTD.
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
- Jun 17, 2016
- Expiry Date
- Jun 17, 2026
About this record
Access comprehensive regulatory information for "joimax" Versicon 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 26485413cc5ee5c64e09e8cb24a8e0e6 and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL 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