Taiwan FDA registration ec4e202280d778dd8cee40433bfccdb5

"Yanbo" spray therapy device

TW: “雃博”噴霧治療器
Taiwan flagTaiwan·Risk Class 2·Wellell Inc.·Registered Nov 23, 2009 – Nov 23, 2019Cancelled
Registration details
Analysis ID
ec4e202280d778dd8cee40433bfccdb5
Customs Code
DHY00500283902
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
Nov 23, 2009
Expiry Date
Nov 23, 2019
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 ec4e202280d778dd8cee40433bfccdb5 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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