Taiwan FDA registration 0203a81385dc7cf0e548175c305a7b3a
“Tekno” Manual Surgical Instrument for General Use (Non-sterile)
TW: “鈦科諾” 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH·Registered May 27, 2016 – May 27, 2021CancelledRegistration details
- Analysis ID
- 0203a81385dc7cf0e548175c305a7b3a
- License Form
- Ministry of Health Medical Device Import No. 016581
- Customs Code
- DHA09401658103
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)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 27, 2016
- Expiry Date
- May 27, 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” 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 0203a81385dc7cf0e548175c305a7b3a and manufactured by TEKNO-MEDICAL OPTIK-CHIRURGIE GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices