Taiwan FDA registration 42141cba0c9c655fe0707a2a5b396cd9

"Guise Ai" middle ear analyzer

TW: “吉斯艾” 中耳分析儀

Taiwan·Risk Class 2·DGS Diagnostics Sp. z o.o.;;DIAGNOSTIC GROUP LLC Doing Business As Grason-Stadler·Registered Nov 24, 2016 – Nov 24, 2026Active

Registration details

Analysis ID: 42141cba0c9c655fe0707a2a5b396cd9
Customs Code: DHA05602897000

Company information

Manufacturer: DGS Diagnostics Sp. z o.o.;;DIAGNOSTIC GROUP LLC Doing Business As Grason-Stadler
Manufacturer Country: United States;;Poland
Authorized Representative: FORMOSA MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1): G ENT Science
Product Type (Level 2): G.1090 Auditory Resistance Checker
Import Information: import

Dates and status

Registration Date: Nov 24, 2016
Expiry Date: Nov 24, 2026

About this record

Access comprehensive regulatory information for "Guise Ai" middle ear analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42141cba0c9c655fe0707a2a5b396cd9 and manufactured by DGS Diagnostics Sp. z o.o.;;DIAGNOSTIC GROUP LLC Doing Business As Grason-Stadler. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS CO., LTD..

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