Taiwan FDA registration 4d27d33577dce52d50f4d78e1bbb99c8
"Shirley" hysteroscopy and its accessories
TW: “雪莉”子宮鏡及其附件
Registration details
- Analysis ID
- 4d27d33577dce52d50f4d78e1bbb99c8
- Customs Code
- DHA00601884801
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.1690 Uterine mirrors and their accessories
- Import Information
- import
Dates and status
- Registration Date
- May 09, 2008
- Expiry Date
- May 09, 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" hysteroscopy and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4d27d33577dce52d50f4d78e1bbb99c8 and manufactured by SCHOLLY FIBEROPTIC GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices