Taiwan FDA registration 91af1f424df1531c4a2269f84de9fad1
RCPA Quality Assurance Programs-Anatomical Pathology (Non-Sterile)
TW: 澳洲皇家病理學院解剖病理學外部品管計劃 (未滅菌)
Taiwan·Risk Class 1·MD·RCPA QUALITY ASSURANCE PROGRAMS PTY LTD·Registered Dec 30, 2013 – Dec 30, 2018CancelledRegistration details
- Analysis ID
- 91af1f424df1531c4a2269f84de9fad1
- License Form
- Ministry of Health Medical Device Import No. 013737
- Customs Code
- DHA09401373706
Company information
- Manufacturer
- RCPA QUALITY ASSURANCE PROGRAMS PTY LTD
- Manufacturer Country
- Australia
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 30, 2013
- Expiry Date
- Dec 30, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for RCPA Quality Assurance Programs-Anatomical Pathology (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 91af1f424df1531c4a2269f84de9fad1 and manufactured by RCPA QUALITY ASSURANCE PROGRAMS PTY LTD. The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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