Taiwan FDA registration 0565ffeab64d878804849d1d8ba9aec8
"Razek" Manual Arthroscopic Instruments (Non-sterile)
TW: "洛賽克" 手動式關節鏡器材(未滅菌)
Taiwan·Risk Class 1·MD·RAZEK EQUIPAMENTOS·Registered Jul 22, 2015 – Jul 22, 2020CancelledRegistration details
- Analysis ID
- 0565ffeab64d878804849d1d8ba9aec8
- License Form
- Ministry of Health Medical Device Import No. 015500
- Customs Code
- DHA09401550001
Company information
- Manufacturer
- RAZEK EQUIPAMENTOS
- Manufacturer Country
- Brazil
- Authorized Representative
- GUO YANG MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 22, 2015
- Expiry Date
- Jul 22, 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 "Razek" Manual Arthroscopic Instruments (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 0565ffeab64d878804849d1d8ba9aec8 and manufactured by RAZEK EQUIPAMENTOS. The authorized representative in Taiwan is GUO YANG MEDICAL CO., LTD..
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