Taiwan FDA registration d37bc11f91641e1371cc8e7b61b473ff

"Cheng Kang" Hearing aids (Non-sterile)

TW: "誠康" 助聽器 (未滅菌)

Taiwan·Risk Class 1·MD·SHENZHEN ZHONGDE HEARINGTECHNOLOGY CO., LTD·Registered Oct 30, 2017 – Oct 30, 2022Expired

Registration details

Analysis ID: d37bc11f91641e1371cc8e7b61b473ff
License Form: Ministry of Health Medical Device Land Transport No. 003258
Customs Code: DHA09600325804

Company information

Manufacturer: SHENZHEN ZHONGDE HEARINGTECHNOLOGY CO., LTD
Manufacturer Country: China
Authorized Representative: TRUE KANG CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
Product Type (Level 1): G ENT device
Product Type (Level 2): G3300 hearing aid
Import Information: Imported from abroad; Made in China

Dates and status

Registration Date: Oct 30, 2017
Expiry Date: Oct 30, 2022

About this record

Access comprehensive regulatory information for "Cheng Kang" Hearing aids (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 d37bc11f91641e1371cc8e7b61b473ff and manufactured by SHENZHEN ZHONGDE HEARINGTECHNOLOGY CO., LTD. The authorized representative in Taiwan is TRUE KANG CO., LTD..

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