Taiwan FDA registration 3fd0f05a23cfdce3e9599e1dca250bce
"Shirley" cystoscopy
TW: “雪莉”膀胱鏡
Taiwan·Risk Class 2·SCHOLLY FIBEROPTIC GMBH·Registered Apr 24, 2008 – Apr 24, 2013CancelledRegistration details
- Analysis ID
- 3fd0f05a23cfdce3e9599e1dca250bce
- Customs Code
- DHA00601882209
Company information
- Manufacturer
- SCHOLLY FIBEROPTIC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- REVO LASER CORPORATION
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.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Apr 24, 2008
- Expiry Date
- Apr 24, 2013
- Cancellation Date
- Jun 11, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Shirley" cystoscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fd0f05a23cfdce3e9599e1dca250bce and manufactured by SCHOLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.
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