Taiwan FDA registration f1b1e242ca5317e6c78b5505163ac5e3
"Middleco" Rhône heavy artificial kidney repetition processing system
TW: “明德科”羅納重人工腎臟重複處理系統
Taiwan·Risk Class 2·MINNTECH CORPORATION·Registered Mar 25, 2011 – Mar 25, 2016CancelledRegistration details
- Analysis ID
- f1b1e242ca5317e6c78b5505163ac5e3
- Customs Code
- DHA00602224002
Company information
- Manufacturer
- MINNTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- FORMOSAN BIOTECH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5600 血液透析用吸附式再生透析系統
- Import Information
- import
Dates and status
- Registration Date
- Mar 25, 2011
- Expiry Date
- Mar 25, 2016
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Middleco" Rhône heavy artificial kidney repetition processing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f1b1e242ca5317e6c78b5505163ac5e3 and manufactured by MINNTECH CORPORATION. The authorized representative in Taiwan is FORMOSAN BIOTECH CO., LTD..
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