Taiwan FDA registration f752b982b00219d16a9a3bf62f3cea58
PBF Double Dyeing Diagnostic Reagent (Non-Sterile)
TW: 寶齡雙重染色診斷試劑(未滅菌)
Taiwan·Risk Class 1·MD·Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- f752b982b00219d16a9a3bf62f3cea58
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 001272
- Customs Code
- DHY08300127201
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PANION & BF BIOTECH INC.
Product details
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1850 Dyes and chemical solution dyes
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for PBF Double Dyeing Diagnostic Reagent (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 f752b982b00219d16a9a3bf62f3cea58 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Medical Equipment Factory. The authorized representative in Taiwan is PANION & BF BIOTECH INC..
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