Taiwan FDA registration 56c9990337df44970bd0f17f72fd60d2
"HERMANN" MANUAL SURGICAL INSTRUMENT FOR GENERAL USE(Non-Sterile)
TW: "賀萌" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·HANS HERMANN GMBH MEDIZINTEHNIK·Registered Apr 16, 2015 – Apr 16, 2020CancelledRegistration details
- Analysis ID
- 56c9990337df44970bd0f17f72fd60d2
- License Form
- Ministry of Health Medical Device Import No. 015120
- Customs Code
- DHA09401512001
Company information
- Manufacturer
- HANS HERMANN GMBH MEDIZINTEHNIK
- Manufacturer Country
- Germany
- Authorized Representative
- GUO YANG MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 16, 2015
- Expiry Date
- Apr 16, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "HERMANN" MANUAL SURGICAL INSTRUMENT FOR GENERAL USE(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 56c9990337df44970bd0f17f72fd60d2 and manufactured by HANS HERMANN GMBH MEDIZINTEHNIK. The authorized representative in Taiwan is GUO YANG MEDICAL CO., LTD..
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