Taiwan FDA registration 7692f8a485cc7d14a3f3f1a458bde7b1

"Freiyfang" hearing aid analyzer

TW: “佛賴伊芳”助聽器分析儀
Taiwan flagTaiwan·Risk Class 2·FRYE ELECTRONICS, INC.·Registered Aug 30, 2011 – Aug 30, 2016Cancelled
Registration details
Analysis ID
7692f8a485cc7d14a3f3f1a458bde7b1
Customs Code
DHA00602276805
Company information
Manufacturer Country
United States
Authorized Representative
GREAT SOUND 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.3310 Hearing Aid Correctors and Analysis Systems
Import Information
import
Dates and status
Registration Date
Aug 30, 2011
Expiry Date
Aug 30, 2016
Cancellation Date
Aug 14, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Freiyfang" hearing aid analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7692f8a485cc7d14a3f3f1a458bde7b1 and manufactured by FRYE ELECTRONICS, INC.. The authorized representative in Taiwan is GREAT SOUND CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FRYE ELECTRONICS, INC., and 2 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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