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"Fujifilm Systems" instrument and equipment protective sleeve (sterilization) - Taiwan Registration a1e17fdbff8c38528fa210a82cdf1509

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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a1e17fdbff8c38528fa210a82cdf1509
Registration Details
Taiwan FDA Registration: a1e17fdbff8c38528fa210a82cdf1509
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Device Details

"Fujifilm Systems" instrument and equipment protective sleeve (sterilization)
TW: โ€œๅฏŒๅฃซ็ณป็ตฑโ€ๅ„€ๅ™จ่ˆ‡่จญๅ‚™ไฟ่ญทๅฅ—(ๆป…่Œ)
Risk Class 1

Registration Details

a1e17fdbff8c38528fa210a82cdf1509

DHA09402092906

Company Information

Product Details

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)".

I General, Plastic Surgery and Dermatology

I.4370 Surgical drapes and accessories

Input;; QMS/QSD

Dates and Status

Oct 07, 2019

Oct 07, 2029