Taiwan FDA registration 7e73d0ff87698b87e5647c7c9855e61c
"Shirley" for laparoscope in obstetrics and gynecology and its appendages
TW: “雪莉”婦產科用腹腔鏡及其附件
Taiwan·Risk Class 2·SCHOLLY FIBEROPTIC GMBH·Registered Feb 05, 2008 – Feb 05, 2013CancelledRegistration details
- Analysis ID
- 7e73d0ff87698b87e5647c7c9855e61c
- Customs Code
- DHA00601859001
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)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1720 Gynecology and gynecologic laparoscopes and their appendages
- Import Information
- import
Dates and status
- Registration Date
- Feb 05, 2008
- Expiry Date
- Feb 05, 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" for laparoscope in obstetrics and gynecology and its appendages in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e73d0ff87698b87e5647c7c9855e61c and manufactured by SCHOLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.
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