Taiwan FDA registration c68b0688fd1f1cb5172af141c0a5a49d
“TSK” STERIJECT Premium Disposable Hypodermic Needle STERiGlide Cannula
TW: “帝斯克”史特滑鈍針
Taiwan·Risk Class 2·MD·TSK LABORATORY, JAPAN, SOJA NO. 1 FACTORY·Registered Nov 29, 2018 – Nov 29, 2023ExpiredRegistration details
- Analysis ID
- c68b0688fd1f1cb5172af141c0a5a49d
- License Form
- Ministry of Health Medical Device Import No. 031853
- Customs Code
- DHA05603185303
Company information
- Manufacturer
- TSK LABORATORY, JAPAN, SOJA NO. 1 FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- AESMED CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5570 Subcutaneous single-lumen needle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 29, 2018
- Expiry Date
- Nov 29, 2023
About this record
Access comprehensive regulatory information for “TSK” STERIJECT Premium Disposable Hypodermic Needle STERiGlide Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c68b0688fd1f1cb5172af141c0a5a49d and manufactured by TSK LABORATORY, JAPAN, SOJA NO. 1 FACTORY. The authorized representative in Taiwan is AESMED CO., LTD..
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