Taiwan FDA registration 5636b645faa96946cf8dbab9d9c62f4b

"Mebi" home treatment humidifier (unsterilized)

TW: “美比”家用治療潮濕器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MEBBY S.P.A.·Registered Jan 31, 2007 – Jan 31, 2012Cancelled
Registration details
Analysis ID
5636b645faa96946cf8dbab9d9c62f4b
Customs Code
DHA04400557109
Company information
Manufacturer
MEBBY S.P.A.
Manufacturer Country
Italy
Authorized Representative
TAIWAN I-CHAN COMPANY
Product details
Intended Use
Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5460 家用治療潮濕器
Import Information
import
Dates and status
Registration Date
Jan 31, 2007
Expiry Date
Jan 31, 2012
Cancellation Date
Apr 30, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Mebi" home treatment humidifier (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5636b645faa96946cf8dbab9d9c62f4b and manufactured by MEBBY S.P.A.. The authorized representative in Taiwan is TAIWAN I-CHAN COMPANY.

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