Taiwan FDA registration 367507f7e02758106357b6297e69acae
"Tengwang" wound treatment kit (unsterilized)
TW: "騰旺"創傷處理包(未滅菌)
Taiwan·Risk Class 1·Tengwang Co., Ltd·Registered Feb 22, 2011 – Feb 22, 2016CancelledRegistration details
- Analysis ID
- 367507f7e02758106357b6297e69acae
Company information
- Manufacturer
- Tengwang Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Tengwang Co., Ltd
Product details
- Intended Use
- It is limited to the first level of the medical device management measures "external use of non-absorbent gauze or sponge balls (I.4014)", "wound/burn dressings for closure (I.4020)" and "medical adhesive tapes and adhesive bandages (J.5240)".
- Product Type (Level 1)
- J General hospital and personal use equipment;; I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- J.5240 Adhesive tapes and adhesive bandages for medical use; I.4020 Wound/burn dressings for closure;; I.4014 Non-absorbent gauze or sponge balls are used externally
- Import Information
- Domestic
Dates and status
- Registration Date
- Feb 22, 2011
- Expiry Date
- Feb 22, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Tengwang" wound treatment kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 367507f7e02758106357b6297e69acae and manufactured by Tengwang Co., Ltd. The authorized representative in Taiwan is Tengwang Co., Ltd.
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