Taiwan FDA registration ed82975cfa354a756ed95257f5709cb4
Titan III Cellulose Acetate Plates (Non-Sterile)
TW: 泰坦三代醋酸纖維片(未滅菌)
Taiwan·Risk Class 1·MD·HELENA LABORATORIES CORP.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- ed82975cfa354a756ed95257f5709cb4
- License Form
- Ministry of Health Medical Device Import Registration No. 001974
- Customs Code
- DHA08400197408
Company information
- Manufacturer
- HELENA LABORATORIES CORP.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Different items can be measured with different buffers and color solutions
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2485 Electrophoresis equipment for clinical use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for Titan III Cellulose Acetate Plates (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 ed82975cfa354a756ed95257f5709cb4 and manufactured by HELENA LABORATORIES CORP.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
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