Taiwan FDA registration 9a11cdbfe5064dc57622e0e0f19ebf3b
Tengwang sputum pack
TW: 騰旺抽痰包
Taiwan·Risk Class 1·ZHANGJIAGANG WENHAO INDUSTRY CO., LTD.·Registered Nov 29, 2005 – Nov 29, 2010CancelledRegistration details
- Analysis ID
- 9a11cdbfe5064dc57622e0e0f19ebf3b
- Customs Code
- DHA04600006702
Company information
- Manufacturer
- ZHANGJIAGANG WENHAO INDUSTRY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- LUXVIEW INTERNATIONAL INC.
Product details
- Intended Use
- The bronchial bronchial suction guide is a device used to extract liquids or semi-solids from the patient's upper airway.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Nov 29, 2005
- Expiry Date
- Nov 29, 2010
- Cancellation Date
- Nov 30, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Tengwang sputum pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a11cdbfe5064dc57622e0e0f19ebf3b and manufactured by ZHANGJIAGANG WENHAO INDUSTRY CO., LTD.. The authorized representative in Taiwan is LUXVIEW INTERNATIONAL INC..
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