Taiwan FDA registration 8b9c4a6e5a27e44066a2110a4788fda1
"LAITEST"SITZ BATH TUB(NON-STERILE)
TW: "萊潔"舒適坐浴盆組(未滅菌)
Taiwan·Risk Class 1·MD·R&R MEDICAL CORPORATION LTD.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 8b9c4a6e5a27e44066a2110a4788fda1
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000495
- Customs Code
- DHY08300049500
Company information
- Manufacturer
- R&R MEDICAL CORPORATION LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- R&R MEDICAL CORPORATION LTD.
Product details
- Intended Use
- Consisting of a bathtub that can hold water, it is used in external hydrotherapy to relieve pain or itching and accelerate the recovery of inflammation and traumatic tissues around the anus or perineum.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5125 Non-powered sitz bath
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "LAITEST"SITZ BATH TUB(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 8b9c4a6e5a27e44066a2110a4788fda1 and manufactured by R&R MEDICAL CORPORATION LTD.. The authorized representative in Taiwan is R&R MEDICAL CORPORATION LTD..
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