Taiwan FDA registration baa629fddf84b91b517e00f37d8418a7
"Gibek" wet ball (artificial nose)
TW: "吉倍克" 潮濕球(人工鼻)
Taiwan·Risk Class 1·RUSCH SDN. BHD.·Registered Dec 21, 2005 – Dec 21, 2010CancelledRegistration details
- Analysis ID
- baa629fddf84b91b517e00f37d8418a7
- Customs Code
- DHA04400229700
Company information
- Manufacturer
- RUSCH SDN. BHD.
- Manufacturer Country
- Malaysia
- Authorized Representative
- WESSON MEDICAL CO., LTD.
Product details
- Intended Use
- A type of pneumatic device that is placed in a tracheostomy (surgical opening of the larynx) or a tracheostomy tube is inserted into the air tube to warm the breath of the patient.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5375 Heat and humidity condenser (artificial nose)
- Import Information
- import
Dates and status
- Registration Date
- Dec 21, 2005
- Expiry Date
- Dec 21, 2010
- Cancellation Date
- Oct 29, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Gibek" wet ball (artificial nose) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number baa629fddf84b91b517e00f37d8418a7 and manufactured by RUSCH SDN. BHD.. The authorized representative in Taiwan is WESSON MEDICAL CO., LTD..
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