Taiwan FDA registration 9c8e3821fbe57633047bfc4580229b0c
"Xinli" disposable ring syringe
TW: “昕力”一次性使用環柄注射器
Taiwan·Risk Class 2·Sunny Medical Device (Shenzhen) Co., Ltd.·Registered Apr 04, 2019 – Apr 04, 2029ActiveRegistration details
- Analysis ID
- 9c8e3821fbe57633047bfc4580229b0c
- Customs Code
- DHA09200100702
Company information
- Manufacturer
- Sunny Medical Device (Shenzhen) Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- CATHERINE CONSULTANTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1650 血管攝影注射器和注射筒
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 04, 2019
- Expiry Date
- Apr 04, 2029
About this record
Access comprehensive regulatory information for "Xinli" disposable ring syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c8e3821fbe57633047bfc4580229b0c and manufactured by Sunny Medical Device (Shenzhen) Co., Ltd.. The authorized representative in Taiwan is CATHERINE CONSULTANTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices