Taiwan FDA registration a1a46bde392880cc946cf6907656e627
“ARKRAY”PocketChem UA PU-4010(Non-Sterile)
TW: “愛科來”尿液分析檢測儀 PU-4010(未滅菌)
Taiwan·Risk Class 1·MD·ARKRAY FACTORY INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- a1a46bde392880cc946cf6907656e627
- License Form
- Ministry of Health Medical Device Import Registration No. 008771
- Customs Code
- DHA08400877103
Company information
- Manufacturer
- ARKRAY FACTORY INC.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDTRI CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for “ARKRAY”PocketChem UA PU-4010(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 a1a46bde392880cc946cf6907656e627 and manufactured by ARKRAY FACTORY INC.. The authorized representative in Taiwan is MEDTRI CO., LTD..
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