Taiwan FDA registration 5cf50f3206ded2f4eed3862b0ccad694
Taisho and autoclaves
TW: 大正和高壓蒸氣滅菌器
Taiwan·Risk Class 2·TA CHENG HO INSTRUMENT CO., LTD.·Registered Mar 23, 2012 – Mar 23, 2027ActiveRegistration details
- Analysis ID
- 5cf50f3206ded2f4eed3862b0ccad694
- Customs Code
- DHY00500362600
Company information
- Manufacturer
- TA CHENG HO INSTRUMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TA CHENG HO INSTRUMENT 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
- Domestic
Dates and status
- Registration Date
- Mar 23, 2012
- Expiry Date
- Mar 23, 2027
About this record
Access comprehensive regulatory information for Taisho and autoclaves in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cf50f3206ded2f4eed3862b0ccad694 and manufactured by TA CHENG HO INSTRUMENT CO., LTD.. The authorized representative in Taiwan is TA CHENG HO INSTRUMENT CO., LTD..
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