Taiwan FDA registration d1e962b381fb34ad45c4a217e891c628

"Akiyama" suture needle for medical treatment (unsterilized)

TW: "秋山"醫療用縫合針 (未滅菌)

Taiwan·Risk Class 1·AKIYAMA MEDICAL MFG. CO. LTD.·Registered Oct 28, 2005 – Oct 28, 2025Expired

Registration details

Analysis ID: d1e962b381fb34ad45c4a217e891c628
Customs Code: DHA04400140103

Company information

Manufacturer: AKIYAMA MEDICAL MFG. CO. LTD.
Manufacturer Country: Japan
Authorized Representative: Yingheng Enterprises Limited

Product details

Intended Use: It is a non-powered, hand-held or hand-operated device that can be reused or thrown away after use, and is used for various general surgeries.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Oct 28, 2005
Expiry Date: Oct 28, 2025

About this record

Access comprehensive regulatory information for "Akiyama" suture needle for medical treatment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1e962b381fb34ad45c4a217e891c628 and manufactured by AKIYAMA MEDICAL MFG. CO. LTD.. The authorized representative in Taiwan is Yingheng Enterprises Limited.

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