Taiwan FDA registration a136193f6a966555afddeaffc7de458b
"Unite" vacuum powered body fluid absorption device (unsterilized)
TW: “優耐特”真空動力式體液吸收器具(未滅菌)
Taiwan·Risk Class 1·Oxygen Machinery Industry Co., Ltd. Guantian Factory·Registered Mar 08, 2010 – Mar 08, 2020CancelledRegistration details
- Analysis ID
- a136193f6a966555afddeaffc7de458b
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Dayi Medical Instrument Factory
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- 國產;; 委託製造;; QMS/QSD
Dates and status
- Registration Date
- Mar 08, 2010
- Expiry Date
- Mar 08, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Unite" vacuum powered body fluid absorption device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a136193f6a966555afddeaffc7de458b and manufactured by Oxygen Machinery Industry Co., Ltd. Guantian Factory. The authorized representative in Taiwan is Dayi Medical Instrument Factory.
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