Taiwan FDA registration 5ba5bb8d13a10980caadda8b0360902b
"Kashiwa Riki" manual instrument for general surgery (unsterilized)
TW: "柏力"一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·BIOLIFE MEDICAL DEVICE INC.·Registered Oct 24, 2011 – Oct 24, 2026ActiveRegistration details
- Analysis ID
- 5ba5bb8d13a10980caadda8b0360902b
Company information
- Manufacturer
- BIOLIFE MEDICAL DEVICE INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOLIFE MEDICAL DEVICE INC.
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 24, 2011
- Expiry Date
- Oct 24, 2026
About this record
Access comprehensive regulatory information for "Kashiwa Riki" manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5ba5bb8d13a10980caadda8b0360902b and manufactured by BIOLIFE MEDICAL DEVICE INC.. The authorized representative in Taiwan is BIOLIFE MEDICAL DEVICE INC..
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