Taiwan FDA registration 95b2485c3550f07f75a15ede8565a82f
"Interwa" Jerry General Manual Instruments for Obstetrics and Gynecology (Unsterilized)
TW: "英特華" 傑瑞婦產科用一般手動器械 (未滅菌)
Taiwan·Risk Class 1·INTEGRA YORK PA, INC.·Registered Aug 01, 2011 – Aug 01, 2021CancelledRegistration details
- Analysis ID
- 95b2485c3550f07f75a15ede8565a82f
- Customs Code
- DHA04401065802
Company information
- Manufacturer
- INTEGRA YORK PA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong 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
- Aug 01, 2011
- Expiry Date
- Aug 01, 2021
- Cancellation Date
- Oct 06, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Interwa" Jerry General Manual Instruments for Obstetrics and Gynecology (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 95b2485c3550f07f75a15ede8565a82f and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is Huizhong Co., Ltd.
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