Taiwan FDA registration 30bbd01ea18b42d2548217867d988323
"Gleich" general manual instruments for obstetrics and gynecology and their accessories (unsterilized)
TW: "格利希" 婦產科用一般手動器械及其附件(未滅菌)
Taiwan·Risk Class 1·QURESHI MANUFACTURING CORPORATION·Registered Apr 14, 2006 – Apr 14, 2016CancelledRegistration details
- Analysis ID
- 30bbd01ea18b42d2548217867d988323
- Customs Code
- DHA04400391900
Company information
- Manufacturer
- QURESHI MANUFACTURING CORPORATION
- Manufacturer Country
- Pakistan
- Authorized Representative
- AK INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "General Manual Instruments for Obstetrics and Gynecology (L.4520)".
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.4520 婦產科用一般手動器械
- Import Information
- import
Dates and status
- Registration Date
- Apr 14, 2006
- Expiry Date
- Apr 14, 2016
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Gleich" general manual instruments for obstetrics and gynecology and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 30bbd01ea18b42d2548217867d988323 and manufactured by QURESHI MANUFACTURING CORPORATION. The authorized representative in Taiwan is AK INSTRUMENTS CO., LTD..
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