Taiwan FDA registration d46d1d684d11cb514364814776e9c818
"Rultract" Cardiovascular surgical instruments (Non-Sterile)
TW: "魯切特"心臟血管外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·RULTRACT INC.·Registered Jun 15, 2015 – Jun 15, 2025ExpiredRegistration details
- Analysis ID
- d46d1d684d11cb514364814776e9c818
- License Form
- Ministry of Health Medical Device Import No. 015340
- Customs Code
- DHA09401534002
Company information
- Manufacturer
- RULTRACT INC.
- Manufacturer Country
- United States
- Authorized Representative
- YOO-HOO Limited
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- 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
- Jun 15, 2015
- Expiry Date
- Jun 15, 2025
About this record
Access comprehensive regulatory information for "Rultract" 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 d46d1d684d11cb514364814776e9c818 and manufactured by RULTRACT INC.. The authorized representative in Taiwan is YOO-HOO Limited.
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