Taiwan FDA registration 636be8a7c05af60740c083c6a2abec2a
"Dybo" Liofilchem LEGIONELLA LATEX KIT (Non-sterile)
TW: "帝博"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·MD·LIOFILCHEM S. R. L.·Registered Nov 02, 2018 – Nov 02, 2023ExpiredRegistration details
- Analysis ID
- 636be8a7c05af60740c083c6a2abec2a
- License Form
- Ministry of Health Medical Device Import No. 019771
- Customs Code
- DHA09401977100
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 devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 02, 2018
- Expiry Date
- Nov 02, 2023
About this record
Access comprehensive regulatory information for "Dybo" Liofilchem LEGIONELLA LATEX KIT (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 636be8a7c05af60740c083c6a2abec2a and manufactured by LIOFILCHEM S. R. L.. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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