Taiwan FDA registration c882d6f2808eed70e089a5e7f22568d7
"Jetti" casing
TW: “捷蒂”套管
Taiwan·Risk Class 2·JEIL TECH CO., LTD.·Registered Mar 09, 2015 – Mar 09, 2030ActiveRegistration details
- Analysis ID
- c882d6f2808eed70e089a5e7f22568d7
- Customs Code
- DHA05602712902
Company information
- Manufacturer
- JEIL TECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CHENG ANN TECHNOLOGY 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)
- J.5570 Subcutaneous single-chamber needle
- Import Information
- import
Dates and status
- Registration Date
- Mar 09, 2015
- Expiry Date
- Mar 09, 2030
About this record
Access comprehensive regulatory information for "Jetti" casing in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c882d6f2808eed70e089a5e7f22568d7 and manufactured by JEIL TECH CO., LTD.. The authorized representative in Taiwan is CHENG ANN TECHNOLOGY CO., LTD..
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