Taiwan FDA registration 37b7bb6d41a0974743b6d5709fb93403
“UroLift” Cystoscope and accessories
TW: “優樂利”膀胱鏡和配件
Taiwan·Risk Class 2·MD·SCHÖLLY FIBEROPTIC GMBH·Registered Feb 17, 2021 – Feb 17, 2026ExpiredRegistration details
- Analysis ID
- 37b7bb6d41a0974743b6d5709fb93403
- License Form
- Ministry of Health Medical Device Import No. 034288
- Customs Code
- DHA05603428800
Company information
- Manufacturer
- SCHÖLLY FIBEROPTIC GMBH
- Manufacturer Country
- Germany
- 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)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2021
- Expiry Date
- Feb 17, 2026
About this record
Access comprehensive regulatory information for “UroLift” Cystoscope and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37b7bb6d41a0974743b6d5709fb93403 and manufactured by SCHÖLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..
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