Taiwan FDA registration af7d7eb926018ff499d1a21ad7d94dae
"LDBIO Diagnostics" Aspergillus Assay (Non-sterile)
TW: "勞迪拜爾" 麴菌屬檢測套組 (未滅菌)
Taiwan·Risk Class 1·MD·LDBIO DIAGNOSTICS·Registered Aug 27, 2019 – Aug 27, 2024ExpiredRegistration details
- Analysis ID
- af7d7eb926018ff499d1a21ad7d94dae
- License Form
- Ministry of Health Medical Device Import No. 020790
- Customs Code
- DHA09402079001
Company information
- Manufacturer
- LDBIO DIAGNOSTICS
- Manufacturer Country
- France
- Authorized Representative
- RECHI CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of koji seroreagent (C.3040) of the measures for the administration of medical equipment.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3040 Koji seroreagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 27, 2019
- Expiry Date
- Aug 27, 2024
About this record
Access comprehensive regulatory information for "LDBIO Diagnostics" Aspergillus Assay (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 af7d7eb926018ff499d1a21ad7d94dae and manufactured by LDBIO DIAGNOSTICS. The authorized representative in Taiwan is RECHI CO., LTD..
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