Taiwan FDA registration 09aa56054a5640e8fa56085486bb7bb9
Yihinda pneumoniae antibody reagent (unsterilized)
TW: 毅欣達肺炎鰴漿菌抗體試劑(未滅菌)
Taiwan·Risk Class 1·WEIFANG KANGHUA BIOTECH CO., LTD·Registered Dec 14, 2010 – Dec 14, 2020CancelledRegistration details
- Analysis ID
- 09aa56054a5640e8fa56085486bb7bb9
- Customs Code
- DHA04600119302
Company information
- Manufacturer
- WEIFANG KANGHUA BIOTECH CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological Reagent (C.3375)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3375 黴漿菌屬血清試劑
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 14, 2010
- Expiry Date
- Dec 14, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Yihinda pneumoniae antibody reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09aa56054a5640e8fa56085486bb7bb9 and manufactured by WEIFANG KANGHUA BIOTECH CO., LTD. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices