Taiwan FDA registration 1b276f6d6cc92b5a723b923b416e7cfc
"Aiychen" adjustable bending guide probe (sterilized)
TW: “艾益辰” 可調式彎曲導引探條 (滅菌)
Taiwan·Risk Class 1·GMMI SDN BHD·Registered May 05, 2022 – May 05, 2027ActiveRegistration details
- Analysis ID
- 1b276f6d6cc92b5a723b923b416e7cfc
- Customs Code
- DHA09402280001
Company information
- Manufacturer
- GMMI SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- DAYCARE HEALTH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- May 05, 2022
- Expiry Date
- May 05, 2027
About this record
Access comprehensive regulatory information for "Aiychen" adjustable bending guide probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b276f6d6cc92b5a723b923b416e7cfc and manufactured by GMMI SDN BHD. The authorized representative in Taiwan is DAYCARE HEALTH CO., LTD..
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