Taiwan FDA registration a6821e11d1d22868b65666c7e26b6c3f

"R&R" Air Pressure-Relief Cushion (Non-Sterile)

TW: "萊禮" 充氣凝膠減壓坐墊(未滅菌)

Taiwan·Risk Class 1·MD·R&R MEDICAL CORPORATION LTD.·Registered Jun 12, 2018 – Jun 12, 2028Active

Registration details

Analysis ID: a6821e11d1d22868b65666c7e26b6c3f
License Form: Ministry of Health Medical Device Manufacturing No. 007300

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 identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3175 floating seat cushion
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jun 12, 2018
Expiry Date: Jun 12, 2028

About this record

Access comprehensive regulatory information for "R&R" Air Pressure-Relief Cushion (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 a6821e11d1d22868b65666c7e26b6c3f and manufactured by R&R MEDICAL CORPORATION LTD.. The authorized representative in Taiwan is R&R MEDICAL CORPORATION LTD..

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