Taiwan FDA registration 797615502736fce248aa0b05e9101707
"VIRCELL" VIRAPID Legionella Culture (Non-Sterile)
TW: "凡賽爾"退伍軍人桿菌快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·VIRCELL, S.L·Registered Aug 29, 2013 – Aug 29, 2018CancelledRegistration details
- Analysis ID
- 797615502736fce248aa0b05e9101707
- License Form
- Ministry of Health Medical Device Import No. 013356
- Customs Code
- DHA09401335607
Company information
- Manufacturer
- VIRCELL, S.L
- Manufacturer Country
- Spain
- Authorized Representative
- Ariel Health Inc
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 29, 2013
- Expiry Date
- Aug 29, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "VIRCELL" VIRAPID Legionella Culture (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 797615502736fce248aa0b05e9101707 and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Ariel Health Inc.
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