Taiwan FDA registration 0dfb608628dd4e970218195cb56ac874
“TAITUNG”Rolling Pad (Non-sterile)
TW: “台同”移位滑板 (未滅菌)
Taiwan·Risk Class 1·MD·Taitong Instrument Co., Ltd. Tainan Factory·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 0dfb608628dd4e970218195cb56ac874
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 001656
Company information
- Manufacturer
- Taitong Instrument Co., Ltd. Tainan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taitong Instrument Co., Ltd. Tainan Factory
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for “TAITUNG”Rolling Pad (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 0dfb608628dd4e970218195cb56ac874 and manufactured by Taitong Instrument Co., Ltd. Tainan Factory. The authorized representative in Taiwan is Taitong Instrument Co., Ltd. Tainan Factory.
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