Taiwan FDA registration cfe9e42ea7e1875b924fb440f977bc7a

"REDA" Eye Pad (Non-Sterile)

TW: "鐳鐽" 護眼貼 (未滅菌)

Taiwan·Risk Class 1·MD·REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD·Registered May 16, 2019 – May 16, 2024Expired

Registration details

Analysis ID: cfe9e42ea7e1875b924fb440f977bc7a
License Form: Ministry of Health Medical Device Import No. 020450
Customs Code: DHA09402045003

Company information

Manufacturer: REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD
Manufacturer Country: Singapore
Authorized Representative: Medical Dragon Ltd.

Product details

Intended Use: Limited to the first level recognition range of eye pads (I.4440) of the medical equipment management method.
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4440 Eye pads
Import Information: Imported from abroad

Dates and status

Registration Date: May 16, 2019
Expiry Date: May 16, 2024

About this record

Access comprehensive regulatory information for "REDA" Eye Pad (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 cfe9e42ea7e1875b924fb440f977bc7a and manufactured by REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD. The authorized representative in Taiwan is Medical Dragon Ltd..

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