Taiwan FDA registration 2ea26956669ef702300834309e579f1f
“MEDIONICS” Peritoneal Dialysis System
TW: “美德”腹膜透析儀
Registration details
- Analysis ID
- 2ea26956669ef702300834309e579f1f
- License Form
- Ministry of Health Medical Device Import No. 025397
- Customs Code
- DHA05602539704
Company information
- Manufacturer
- Medionics International Inc.
- Manufacturer Country
- Canada
- Authorized Representative
- Heyan Technology Co., Ltd
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5630 Peritoneal dialysis systems and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 02, 2013
- Expiry Date
- Sep 02, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “MEDIONICS” Peritoneal Dialysis System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2ea26956669ef702300834309e579f1f and manufactured by Medionics International Inc.. The authorized representative in Taiwan is Heyan Technology 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