Taiwan FDA registration c64510d5c37bd95bf30899654d2ed3f3
"Maquet" Cardiovascular Surgical Instruments (Non-Sterile)
TW: "馬克"心臟血管外科器械(未滅菌)
Taiwan·Risk Class 1·MD·MAQUET CARDIOVASCULAR LLC·Registered Oct 27, 2014 – Oct 27, 2019CancelledRegistration details
- Analysis ID
- c64510d5c37bd95bf30899654d2ed3f3
- License Form
- Ministry of Health Medical Device Import No. 014610
- Customs Code
- DHA09401461000
Company information
- Manufacturer
- MAQUET CARDIOVASCULAR LLC
- Manufacturer Country
- United States
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
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
- Oct 27, 2014
- Expiry Date
- Oct 27, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Maquet" 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 c64510d5c37bd95bf30899654d2ed3f3 and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
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