Taiwan FDA registration 29580fc77f9cecc2395cbbadc4313f28
“RUSCH” Simplastic Suprapubic Puncture Instrument
TW: “路希”辛巴司提恥骨上穿刺器
Taiwan·Risk Class 2·MD·TELEFLEX MEDICAL SDN. BHD.·Registered Sep 11, 2018 – Sep 11, 2023ExpiredRegistration details
- Analysis ID
- 29580fc77f9cecc2395cbbadc4313f28
- License Form
- Ministry of Health Medical Device Import No. 031621
- Customs Code
- DHA05603162108
Company information
- Manufacturer
- TELEFLEX MEDICAL SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5090 Suprapubic catheters and their appendages
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 11, 2018
- Expiry Date
- Sep 11, 2023
About this record
Access comprehensive regulatory information for “RUSCH” Simplastic Suprapubic Puncture Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 29580fc77f9cecc2395cbbadc4313f28 and manufactured by TELEFLEX MEDICAL SDN. BHD.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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