Taiwan FDA registration f7f4b4972dfd6ac83196c0d52afd5dc0

"Yanbo" spray therapy device

TW: “雃博”噴霧治療器
Taiwan flagTaiwan·Risk Class 2·Wellell Inc.·Registered Dec 04, 2009 – Dec 04, 2014Cancelled
Registration details
Analysis ID
f7f4b4972dfd6ac83196c0d52afd5dc0
Customs Code
DHY00500284701
Company information
Manufacturer
Wellell Inc.
Manufacturer Country
Taiwan, Province of China
Authorized Representative
Wellell Inc.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5630 Nebulizer
Import Information
Domestic
Dates and status
Registration Date
Dec 04, 2009
Expiry Date
Dec 04, 2014
Cancellation Date
Jun 08, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Yanbo" spray therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f7f4b4972dfd6ac83196c0d52afd5dc0 and manufactured by Wellell Inc.. The authorized representative in Taiwan is Wellell Inc..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Wellell Inc., Jibo Co., Ltd.;; APEX MEDICAL (KUNSHAN) CORP., and 5 recent registrations in the same category. 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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