Taiwan FDA registration a1e17fdbff8c38528fa210a82cdf1509
"Fujifilm Systems" instrument and equipment protective sleeve (sterilization)
TW: “富士系統”儀器與設備保護套(滅菌)
Taiwan·Risk Class 1·Fuji Systems Corporation, Shirakawa Plant·Registered Oct 07, 2019 – Oct 07, 2029ActiveRegistration details
- Analysis ID
- a1e17fdbff8c38528fa210a82cdf1509
- Customs Code
- DHA09402092906
Company information
- Manufacturer
- Fuji Systems Corporation, Shirakawa Plant
- Manufacturer Country
- Japan
- Authorized Representative
- Meide Medical Devices Co., Ltd
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Classification and Grading of Medical Devices "Surgical Covering Cloths and Their Accessories (I.4370)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4370 Surgical drapes and accessories
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 07, 2019
- Expiry Date
- Oct 07, 2029
About this record
Access comprehensive regulatory information for "Fujifilm Systems" instrument and equipment protective sleeve (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a1e17fdbff8c38528fa210a82cdf1509 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is Meide Medical Devices Co., Ltd.
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