Taiwan FDA registration e11f2cc93aa433dc6ab40061b1cd352d
Timera subcutaneous single-chamber needle (sterilized)
TW: 提美拉皮下單腔針（滅菌）
Taiwan·Risk Class 2·SHINEO TECHNOLOGY CO., LTD.·Registered Sep 29, 2023 – Sep 29, 2028ActiveRegistration details
- Analysis ID
- e11f2cc93aa433dc6ab40061b1cd352d
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DIAMOND BIOTECHNOLOGY CO., LTD.
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.5570 Subcutaneous single-chamber needle
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Sep 29, 2023
- Expiry Date
- Sep 29, 2028
About this record
Access comprehensive regulatory information for Timera subcutaneous single-chamber needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e11f2cc93aa433dc6ab40061b1cd352d and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY CO., LTD..
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