Taiwan FDA registration f02e9c01f5cf2157a141009bdd190bc3
Pocketchem UA "Arkray"(PU-4010) (Non-Sterile)
TW: "愛科來"尿液分析檢測儀(未滅菌)
Taiwan·Risk Class 1·MD·Arkray Factory Inc., Head office factory·Registered Oct 01, 2021 – Oct 31, 2027ActiveRegistration details
- Analysis ID
- f02e9c01f5cf2157a141009bdd190bc3
- License Form
- Ministry of Health Medical Device Import Registration No. 005354
- Customs Code
- DHA08400535401
Company information
- Manufacturer
- Arkray Factory Inc., Head office factory
- Manufacturer Country
- Japan
- Authorized Representative
- SYNGEN BIOTECH 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
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2027
About this record
Access comprehensive regulatory information for Pocketchem UA "Arkray"(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 f02e9c01f5cf2157a141009bdd190bc3 and manufactured by Arkray Factory Inc., Head office factory. The authorized representative in Taiwan is SYNGEN BIOTECH CO., LTD..
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