Taiwan FDA registration 98c6e5fe9731f209df7a296f860f756d
Stryker inflatable tourniquet (non-sterile)
TW: "史賽克" 充氣式止血帶(未滅菌)
Registration details
- Analysis ID
- 98c6e5fe9731f209df7a296f860f756d
- Customs Code
- DHA09402364303
Company information
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- Stryker (Far East) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Inflatable Tourniquet (I.5910)" of the classification and grading management measures for medical equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5910 充氣式止血帶
- Import Information
- 委託製造;; 輸入;; QMS/QSD
Dates and status
- Registration Date
- Oct 25, 2024
- Expiry Date
- Oct 25, 2029
About this record
Access comprehensive regulatory information for Stryker inflatable tourniquet (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98c6e5fe9731f209df7a296f860f756d and manufactured by STRYKER INSTRUMENTS;; IMED Medical Mexicana, S. de R.L. de C. V.. The authorized representative in Taiwan is Stryker (Far East) Co., Ltd. Taiwan Branch.
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