Taiwan FDA registration 4cc777bb4fb2e2430f3ca585aa310cdd
REXICARE AIR ACTIVATED HEAT PATCH (Non-sterile)
TW: 瑞斯 溫熱敷貼片(未滅菌)
Taiwan·Risk Class 1·MD·R&R MEDICAL CORPORATION LTD.·Registered Feb 09, 2018 – Feb 09, 2023ExpiredRegistration details
- Analysis ID
- 4cc777bb4fb2e2430f3ca585aa310cdd
- License Form
- Ministry of Health Medical Device Manufacturing No. 007109
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
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Discardable Hot and Cold Compress Packs for Medical Use (O.5710)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5710 Discardable Hot and Cold Compress for Medical Use
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 09, 2018
- Expiry Date
- Feb 09, 2023
About this record
Access comprehensive regulatory information for REXICARE AIR ACTIVATED HEAT PATCH (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 4cc777bb4fb2e2430f3ca585aa310cdd and manufactured by R&R MEDICAL CORPORATION LTD.. The authorized representative in Taiwan is R&R MEDICAL CORPORATION LTD..
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