Taiwan FDA registration 4ab0e082b5218d2f757e420a1c607cbb
Legionella latex agglutination kit (unsterilized)
TW: 〝立飛旋〞退伍軍人桿菌屬乳膠凝集試劑套組 (未滅菌)
Taiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Aug 30, 2011 – Aug 30, 2016CancelledRegistration details
- Analysis ID
- 4ab0e082b5218d2f757e420a1c607cbb
- Customs Code
- DHA04401077506
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3300 嗜血桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Aug 30, 2011
- Expiry Date
- Aug 30, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Legionella latex agglutination kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4ab0e082b5218d2f757e420a1c607cbb and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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