Taiwan FDA registration 710591b3dedf322edb29ab03a1630391
"Taniboku" gynecological general manual instrument (not sterilized)
TW: “谷伯”婦科用一般手動器械 （未滅菌）
Taiwan·Risk Class 1·COOPER SURGICAL INC.·Registered Jun 06, 2006 – Jun 06, 2021CancelledRegistration details
- Analysis ID
- 710591b3dedf322edb29ab03a1630391
- Customs Code
- DHA04400465701
Company information
- Manufacturer
- COOPER SURGICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
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
- Jun 06, 2006
- Expiry Date
- Jun 06, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Taniboku" gynecological general manual instrument (not sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 710591b3dedf322edb29ab03a1630391 and manufactured by COOPER SURGICAL INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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