Taiwan FDA registration ca78e614af467d1ed78457ae51bc5227
"nal von minden" Legionella Urinary Antigen Rapid Test (Non-Sterile)
TW: "納佛明頓" 退伍軍人肺炎尿液抗原快速檢測試劑 (未滅菌)
Registration details
- Analysis ID
- ca78e614af467d1ed78457ae51bc5227
- License Form
- Ministry of Health Medical Device Import No. 015613
- Customs Code
- DHA09401561301
Company information
- Manufacturer
- NAL VON MINDEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- YOULUM BIOTECHNOLOGY CO., LTD.
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 28, 2015
- Expiry Date
- Aug 28, 2020
- Cancellation Date
- Mar 27, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "nal von minden" Legionella Urinary Antigen Rapid Test (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 ca78e614af467d1ed78457ae51bc5227 and manufactured by NAL VON MINDEN GMBH. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., LTD..
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