Taiwan FDA registration 62dfb73344636e12377fda72424a8612
"Sysmex" Fully Automated Urine Particle Digital Imaging Device (Non-sterile)
TW: "希森美康" 全自動尿沉渣數位影像設備(未滅菌)
Taiwan·Risk Class 1·MD·SYSMEX CORPORATION, I-SQUARE·Registered Jun 05, 2018 – Jun 05, 2023CancelledRegistration details
- Analysis ID
- 62dfb73344636e12377fda72424a8612
- License Form
- Ministry of Health Medical Device Import No. 019132
- Customs Code
- DHA09401913202
Company information
- Manufacturer
- SYSMEX CORPORATION, I-SQUARE
- Manufacturer Country
- Japan
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2900 Automated Urinalysis System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 05, 2018
- Expiry Date
- Jun 05, 2023
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "Sysmex" Fully Automated Urine Particle Digital Imaging Device (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 62dfb73344636e12377fda72424a8612 and manufactured by SYSMEX CORPORATION, I-SQUARE. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
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