Taiwan FDA registration e257118a5336cc20aa6e9f9abad81c19
"Tengwang" sterilized sputum pack
TW: "騰旺"滅菌抽痰包
Taiwan·Risk Class 1·ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.·Registered Jun 29, 2007 – Jun 29, 2017CancelledRegistration details
- Analysis ID
- e257118a5336cc20aa6e9f9abad81c19
- Customs Code
- DHA04600039901
Company information
- Manufacturer Country
- China
- Authorized Representative
- Tengwang Co., Ltd
Product details
- Intended Use
- Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jun 29, 2007
- Expiry Date
- Jun 29, 2017
- Cancellation Date
- Nov 22, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Tengwang" sterilized 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 e257118a5336cc20aa6e9f9abad81c19 and manufactured by ZHANGJIAGANG HUAXING RUBBER-PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is Tengwang Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices