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"Mebi" home treatment humidifier (unsterilized) - Taiwan Registration 5636b645faa96946cf8dbab9d9c62f4b

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5636b645faa96946cf8dbab9d9c62f4b
Registration Details
Taiwan FDA Registration: 5636b645faa96946cf8dbab9d9c62f4b
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Device Details

"Mebi" home treatment humidifier (unsterilized)
TW: โ€œ็พŽๆฏ”โ€ๅฎถ็”จๆฒป็™‚ๆฝฎๆฟ•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

5636b645faa96946cf8dbab9d9c62f4b

DHA04400557109

Company Information

Italy

Product Details

Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Household Treatment Moisturizer (D.5460)".

D Anesthesiology

D.5460 ๅฎถ็”จๆฒป็™‚ๆฝฎๆฟ•ๅ™จ

import

Dates and Status

Jan 31, 2007

Jan 31, 2012

Apr 30, 2014

Cancellation Information

Logged out

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