Taiwan FDA registration d24e85760d35a7877476e24169e0582c

"PERSBRA" Radiation Protection Device (Non-Sterile)

TW: "百褓" 輻射防護用具 (未滅菌)

Taiwan·Risk Class 1·MD·Xinghe Biomedical Co., Ltd. Taichung Factory·Registered Oct 19, 2018 – Oct 19, 2023Expired

Registration details

Analysis ID: d24e85760d35a7877476e24169e0582c
License Form: Ministry of Health Medical Device Manufacturing No. 007487

Company information

Manufacturer: Xinghe Biomedical Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BOSOMEER BIOTECH LTD

Product details

Product Type (Level 1): P Devices for radiology
Product Type (Level 2): P6500 Personal Shield
Import Information: Produced in Taiwan, China; Contract manufacturing

Dates and status

Registration Date: Oct 19, 2018
Expiry Date: Oct 19, 2023
Cancellation Date: Jun 27, 2023

About this record

Access comprehensive regulatory information for "PERSBRA" Radiation Protection Device (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 d24e85760d35a7877476e24169e0582c and manufactured by Xinghe Biomedical Co., Ltd. Taichung Factory. The authorized representative in Taiwan is BOSOMEER BIOTECH LTD.

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