Taiwan FDA registration 89e9673cd824fe54ecb9a4b9979b43e4
"Buffalo Filter"Manual Surgical Instrument for General Use (Non-Sterile)
TW: "巴芙洛"一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·BUFFALO FILTER LLC·Registered Dec 27, 2018 – Dec 27, 2023ExpiredRegistration details
- Analysis ID
- 89e9673cd824fe54ecb9a4b9979b43e4
- License Form
- Ministry of Health Medical Device Import No. 019973
- Customs Code
- DHA09401997309
Company information
- Manufacturer
- BUFFALO FILTER LLC
- Manufacturer Country
- United States
- Authorized Representative
- Huizhong Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 27, 2018
- Expiry Date
- Dec 27, 2023
About this record
Access comprehensive regulatory information for "Buffalo Filter"Manual Surgical Instrument for General Use (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 89e9673cd824fe54ecb9a4b9979b43e4 and manufactured by BUFFALO FILTER LLC. The authorized representative in Taiwan is Huizhong Co., Ltd.
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