Taiwan FDA registration 12b82f1ab1383276e99852a9b075be5b
Muto's Stain Reagent Kits for Clinic Pathology (Non-Sterile)
TW: 武藤臨床病理染色試劑組(未滅菌)
Registration details
- Analysis ID
- 12b82f1ab1383276e99852a9b075be5b
- License Form
- Ministry of Health Medical Device Import Registration No. 001943
- Customs Code
- DHA08400194300
Company information
- Manufacturer
- MUTO PURE CHEMICALS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- CHIN I PAO CO., LTD.
Product details
- Intended Use
- Staining cells or tissues for pathological diagnosis.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1850 Dyes and chemical solution dyes
- 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 Muto's Stain Reagent Kits for Clinic Pathology (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 12b82f1ab1383276e99852a9b075be5b and manufactured by MUTO PURE CHEMICALS CO., LTD.. The authorized representative in Taiwan is CHIN I PAO CO., LTD..
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