Taiwan FDA registration ccf9252a3db276fb6209cac2845942cc
"MIYABI" Speculum and accessories (Non-Sterile)
TW: "米亞彼" 檢查鏡及其附件(未滅菌)
Taiwan·Risk Class 1·MD·MIYABI INTERNATIONAL INC.·Registered Jun 12, 2015 – Jun 12, 2020CancelledRegistration details
- Analysis ID
- ccf9252a3db276fb6209cac2845942cc
- License Form
- Ministry of Health Medical Device Import No. 015334
- Customs Code
- DHA09401533407
Company information
- Manufacturer
- MIYABI INTERNATIONAL INC.
- Manufacturer Country
- Japan
- Authorized Representative
- Huixing Co., Ltd
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I1800 inspection mirror and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 12, 2015
- Expiry Date
- Jun 12, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "MIYABI" Speculum and accessories (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 ccf9252a3db276fb6209cac2845942cc and manufactured by MIYABI INTERNATIONAL INC.. The authorized representative in Taiwan is Huixing Co., Ltd.
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