Taiwan FDA registration aa815e78cee83d18c5fe4dbecad05a3e
CapitaLand steam sterilizer
TW: “凱德醫療”蒸氣滅菌器
Taiwan·Risk Class 2·ZHEJIANG GETIDY MEDICAL INSTRUMENT CO., LTD.·Registered Mar 30, 2020 – Mar 30, 2030ActiveRegistration details
- Analysis ID
- aa815e78cee83d18c5fe4dbecad05a3e
- Customs Code
- DHA09200115109
Company information
- Manufacturer
- ZHEJIANG GETIDY MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- KAO TECH MD 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.6880 Sterilizer for steam
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 30, 2020
- Expiry Date
- Mar 30, 2030
About this record
Access comprehensive regulatory information for CapitaLand steam sterilizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa815e78cee83d18c5fe4dbecad05a3e and manufactured by ZHEJIANG GETIDY MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is KAO TECH MD CO., LTD..
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