Taiwan FDA registration 9d423eb0ac27ed0dc23df2ae1aa04a4a

Rystora Adhesive Remover- Spray (Non-Sterile)

TW: 美得膚噴霧除膠劑(未滅菌)

Taiwan·Risk Class 1·MD·FORTUNE MEDICAL INSTRUMENT CORP.·Registered Jul 11, 2022 – Jul 11, 2027Active

Registration details

Analysis ID: 9d423eb0ac27ed0dc23df2ae1aa04a4a
License Form: Ministry of Health Medical Device Manufacturing No. 009621

Company information

Manufacturer: FORTUNE MEDICAL INSTRUMENT CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FORTUNE MEDICAL INSTRUMENT CORP.

Product details

Intended Use: Limited to the classification and grading management of medical devices, the first level of identification range of "surgical skin degreasing agent or deadhesive (I.4730)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I4730 Surgical skin degreasing or de-adhesive
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jul 11, 2022
Expiry Date: Jul 11, 2027

About this record

Access comprehensive regulatory information for Rystora Adhesive Remover- Spray (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 9d423eb0ac27ed0dc23df2ae1aa04a4a and manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. The authorized representative in Taiwan is FORTUNE MEDICAL INSTRUMENT CORP..

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