Taiwan FDA registration 03b752a5f91d8efd47f658ecef21d9c6
"Tontarra" Manual surgical instruments (Non-Sterile)
TW: "通特拉" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·TONTARRA MEDIZINTECHNIK GMBH·Registered Nov 07, 2017 – Nov 07, 2022ExpiredRegistration details
- Analysis ID
- 03b752a5f91d8efd47f658ecef21d9c6
- License Form
- Ministry of Health Medical Device Import No. 018475
- Customs Code
- DHA09401847501
Company information
- Manufacturer
- TONTARRA MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SMARTECH MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- 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
- Nov 07, 2017
- Expiry Date
- Nov 07, 2022
About this record
Access comprehensive regulatory information for "Tontarra" Manual 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 03b752a5f91d8efd47f658ecef21d9c6 and manufactured by TONTARRA MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..
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