Taiwan FDA registration d3795e3603a7d94b28ff64a5f0c1ae9f
"TEKNO" Cardiovascular Surgical Instruments (Non-Sterile)
TW: "德科隆"心臟血管外科器械(未滅菌)
Taiwan·Risk Class 1·MD·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH·Registered Jan 28, 2015 – Jan 28, 2020CancelledRegistration details
- Analysis ID
- d3795e3603a7d94b28ff64a5f0c1ae9f
- License Form
- Ministry of Health Medical Device Import No. 014878
- Customs Code
- DHA09401487803
Company information
- Manufacturer
- TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDITEK LIFESCIENCES CORP.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4500 Cardiovascular Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 28, 2015
- Expiry Date
- Jan 28, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "TEKNO" Cardiovascular Surgical 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 d3795e3603a7d94b28ff64a5f0c1ae9f and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH. The authorized representative in Taiwan is MEDITEK LIFESCIENCES CORP..
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