Taiwan FDA registration eed89a1f61aea454db562be0ce095a64
NITTOBO LDH (Non-Sterile)
TW: 日東紡乳酸脫氫酶檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER·Registered Jul 29, 2019 – Jul 29, 2024ExpiredRegistration details
- Analysis ID
- eed89a1f61aea454db562be0ce095a64
- License Form
- Ministry of Health Medical Device Import No. 020691
- Customs Code
- DHA09402069102
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of lactate dehydrogenase test system (A.1440) of the management method for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1440 Lactate dehydrogenase test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 29, 2019
- Expiry Date
- Jul 29, 2024
About this record
Access comprehensive regulatory information for NITTOBO LDH (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 eed89a1f61aea454db562be0ce095a64 and manufactured by NITTOBO MEDICAL CO., LTD. MEDICAL DEVELOPMENT CENTER. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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