Taiwan FDA registration 2d3619e7b0692b3f84909cb49cce8a02
"Taiwan Tong" bath push bed (unsterilized)
TW: “台同”洗澡推床 (未滅菌)
Taiwan·Risk Class 1·Taitong Instrument Co., Ltd. Tainan Factory·Registered Oct 05, 2006 – Oct 05, 2026ActiveRegistration details
- Analysis ID
- 2d3619e7b0692b3f84909cb49cce8a02
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 identification scope of the "Non-AC Power Patient Lift (J.5510)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5510 Non-AC electric patient lifts
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 05, 2006
- Expiry Date
- Oct 05, 2026
About this record
Access comprehensive regulatory information for "Taiwan Tong" bath push bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d3619e7b0692b3f84909cb49cce8a02 and manufactured by Taitong Instrument Co., Ltd. Tainan Factory. The authorized representative in Taiwan is Taitong Instrument Co., Ltd. Tainan Factory.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices