Taiwan FDA registration 223795f42bb9bacc194950bf3b731bb8

"Meili" air-guided hearing aids (unsterilized)

TW: “美律”氣導式助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MERRY ELECTRONICS (SHENZHEN) CORPORATE LIMITED.·Registered Feb 25, 2014 – Feb 25, 2019Cancelled
Registration details
Analysis ID
223795f42bb9bacc194950bf3b731bb8
Customs Code
DHA09600207708
Company information
Manufacturer Country
China
Authorized Representative
MERRY ELECTRONICS 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 Science
Product Type (Level 2)
G.3300 Hearing Aids
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Feb 25, 2014
Expiry Date
Feb 25, 2019
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Meili" air-guided hearing aids (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 223795f42bb9bacc194950bf3b731bb8 and manufactured by MERRY ELECTRONICS (SHENZHEN) CORPORATE LIMITED.. The authorized representative in Taiwan is MERRY ELECTRONICS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hengxin Medical Equipment Co., Ltd, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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