Taiwan FDA registration 055717bd61c84d3a1243c06b8e857bcb
"Retik" electrotherapy device
TW: “雷蒂克” 電位治療器
Taiwan·Risk Class 2·RELTEC Medical Devices Corporation·Registered Aug 18, 2024 – Aug 18, 2029ActiveRegistration details
- Analysis ID
- 055717bd61c84d3a1243c06b8e857bcb
- Customs Code
- DHA05603728700
Company information
- Manufacturer
- RELTEC Medical Devices Corporation
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.0001 靜電器(電位治療器)
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2024
- Expiry Date
- Aug 18, 2029
About this record
Access comprehensive regulatory information for "Retik" electrotherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 055717bd61c84d3a1243c06b8e857bcb and manufactured by RELTEC Medical Devices Corporation. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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