Taiwan FDA registration 440473581dde793059b5a789721ce6d7
“TSK” Steriject Hypodermic Needle CSH Cannula
TW: “帝斯克”鈍針
Taiwan·Risk Class 2·MD·TSK LABORATORY, JAPAN, SOJA NO. 1 FACTORY·Registered Nov 23, 2015 – Nov 23, 2025ExpiredRegistration details
- Analysis ID
- 440473581dde793059b5a789721ce6d7
- License Form
- Ministry of Health Medical Device Import No. 027954
- Customs Code
- DHA05602795407
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 23, 2015
- Expiry Date
- Nov 23, 2025
About this record
Access comprehensive regulatory information for “TSK” Steriject Hypodermic Needle CSH Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 440473581dde793059b5a789721ce6d7 and manufactured by TSK LABORATORY, JAPAN, SOJA NO. 1 FACTORY. The authorized representative in Taiwan is AESMED CO., LTD..
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