Taiwan FDA registration 7aeedbb17e66652912a7bd9e1d0d9205
"Tekno" Speculum and accessories (Non-Sterile)
TW: "鈦科諾" 檢查鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.·Registered Jul 21, 2016 – Jul 21, 2021CancelledRegistration details
- Analysis ID
- 7aeedbb17e66652912a7bd9e1d0d9205
- License Form
- Ministry of Health Medical Device Import No. 016798
- Customs Code
- DHA09401679802
Company information
- Manufacturer
- TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.
- Manufacturer Country
- Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
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
- Jul 21, 2016
- Expiry Date
- Jul 21, 2021
- Cancellation Date
- Aug 09, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Tekno" 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 7aeedbb17e66652912a7bd9e1d0d9205 and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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