Taiwan FDA registration 4f9e386919c2becd811c7a539ac74ce9
LUMARK HEALTHCARE Pneumatic tourniquet (Non-Sterile)
TW: 眾億 充氣式止血帶 (未滅菌)
Taiwan·Risk Class 1·MD·Zhongyi Industrial Co., Ltd. new housing factory·Registered Nov 21, 2018 – Nov 21, 2023ExpiredRegistration details
- Analysis ID
- 4f9e386919c2becd811c7a539ac74ce9
- License Form
- Ministry of Health Medical Device Manufacturing No. 007533
Company information
- Manufacturer
- Zhongyi Industrial Co., Ltd. new housing factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Zhongyi Industrial Co., Ltd. new housing factory
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I5910 Inflatable tourniquet
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 21, 2018
- Expiry Date
- Nov 21, 2023
About this record
Access comprehensive regulatory information for LUMARK HEALTHCARE Pneumatic tourniquet (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 4f9e386919c2becd811c7a539ac74ce9 and manufactured by Zhongyi Industrial Co., Ltd. new housing factory. The authorized representative in Taiwan is Zhongyi Industrial Co., Ltd. new housing factory.
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