Taiwan FDA registration d99c249f29434fb0f8e3cdad699548bd
Nafoss hollow fibrous artificial kidney
TW: 納富斯空心纖維型人工腎臟
Registration details
- Analysis ID
- d99c249f29434fb0f8e3cdad699548bd
- Customs Code
- DHA00600452006
Company information
- Manufacturer
- ORGANON TEKNIKA B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- Aujialon AG
Product details
- Product Type (Level 1)
- 0333 Dialysis tube (artificial kidney)
- Import Information
- import
Dates and status
- Registration Date
- Jan 10, 1987
- Expiry Date
- Mar 11, 2010
- Cancellation Date
- Dec 07, 1992
Cancellation information
- Status
- Logged out
- Reason
- 有效期間已屆未能補件
About this record
Access comprehensive regulatory information for Nafoss hollow fibrous artificial kidney in Taiwan's medical device market through Pure Global AI's free database. is registered under number d99c249f29434fb0f8e3cdad699548bd and manufactured by ORGANON TEKNIKA B.V.. The authorized representative in Taiwan is Aujialon AG.
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