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"Bonthe" otolaryngology foam (sterilization) - Taiwan Registration f054dbe6680c3718ab92392b205e2bc7

Access comprehensive regulatory information for "Bonthe" otolaryngology foam (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f054dbe6680c3718ab92392b205e2bc7 and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is BIOTEQUE CORPORATION.

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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f054dbe6680c3718ab92392b205e2bc7
Registration Details
Taiwan FDA Registration: f054dbe6680c3718ab92392b205e2bc7
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Device Details

"Bonthe" otolaryngology foam (sterilization)
TW: "้‚ฆ็‰น" ่€ณ้ผปๅ–‰็ง‘็”จๆณกๆฃ‰ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f054dbe6680c3718ab92392b205e2bc7

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of "external use of non-absorbent gauze or sponge balls (I.4014)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4014 Non-absorbent cloth or sea balls are used externally

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Dates and Status

Dec 01, 2016

Dec 01, 2021

Sep 11, 2023

Cancellation Information

Logged out

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