Taiwan FDA registration 7a03f6d42b21f8abed3716b850726f14
"OKmeter"Hearing Aid (Non-Sterile)
TW: "歐克"助聽器(未滅菌)
Taiwan·Risk Class 1·MD·OK BIOTECH CO., LTD.·Registered Feb 21, 2020 – Feb 21, 2025ExpiredRegistration details
- Analysis ID
- 7a03f6d42b21f8abed3716b850726f14
- License Form
- Ministry of Health Medical Device Manufacturing No. 008205
Company information
- Manufacturer
- OK BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- OK BIOTECH CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 21, 2020
- Expiry Date
- Feb 21, 2025
- Cancellation Date
- Jan 05, 2023
About this record
Access comprehensive regulatory information for "OKmeter"Hearing Aid (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 7a03f6d42b21f8abed3716b850726f14 and manufactured by OK BIOTECH CO., LTD.. The authorized representative in Taiwan is OK BIOTECH CO., LTD..
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