Taiwan FDA registration 4f31683ede5d0dcce99ee4f0e2fe419e
“RUSCH” SILASIL foley catheters
TW: “路希”希拉夕爾導尿管
Taiwan·Risk Class 2·MD·Teleflex Medical Sdn.Bhd.·Registered May 13, 2015 – May 13, 2020CancelledRegistration details
- Analysis ID
- 4f31683ede5d0dcce99ee4f0e2fe419e
- License Form
- Ministry of Health Medical Device Import No. 027387
- Customs Code
- DHA05602738701
Company information
- Manufacturer
- Teleflex Medical Sdn.Bhd.
- Manufacturer Country
- Malaysia
- Authorized Representative
- TELEFLEX MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5130 Urinary catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 13, 2015
- Expiry Date
- May 13, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “RUSCH” SILASIL foley catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f31683ede5d0dcce99ee4f0e2fe419e and manufactured by Teleflex Medical Sdn.Bhd.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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