Taiwan FDA registration 98aba356654d30b5c0b4852ec0d1c9a8
"Sterr" sterilized packaging
TW: “斯德瑞”滅菌包裝
Registration details
- Analysis ID
- 98aba356654d30b5c0b4852ec0d1c9a8
- Customs Code
- DHA09200136900
Company information
- Manufacturer
- Sterivic Medical Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- SUNDENT CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6850 sterilization kit
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 16, 2022
- Expiry Date
- Jun 16, 2027
About this record
Access comprehensive regulatory information for "Sterr" sterilized packaging in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98aba356654d30b5c0b4852ec0d1c9a8 and manufactured by Sterivic Medical Co., Ltd.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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