Taiwan FDA registration 9995217e0fe03efd58a4d9bc91832bc3

"T. Matsui" Ear, nose, and throat manual surgical instrument (Non-Sterile)

TW: "崧景" 耳鼻喉手動式外科器械 (未滅菌)

Taiwan·Risk Class 1·MD·TM MATSUI CO., LTD.·Registered Mar 05, 2021 – Mar 05, 2026Expired

Registration details

Analysis ID: 9995217e0fe03efd58a4d9bc91832bc3
License Form: Ministry of Health Medical Device Import No. 022364
Customs Code: DHA09402236407

Company information

Manufacturer: TM MATSUI CO., LTD.
Manufacturer Country: Japan
Authorized Representative: GOLDENSPRING MEDI-TECH CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G4420 OTOLARYNGARY Manual Surgical Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 05, 2021
Expiry Date: Mar 05, 2026

About this record

Access comprehensive regulatory information for "T. Matsui" Ear, nose, and throat manual surgical instrument (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 9995217e0fe03efd58a4d9bc91832bc3 and manufactured by TM MATSUI CO., LTD.. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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