Taiwan FDA registration 5485d014f87d6ee251dcbc23aa30dc1e

“OMRON” Compressor Nebulizer

TW: “歐姆龍” 噴霧器
Taiwan flagTaiwan·Risk Class 2·MD·OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.·Registered Nov 21, 2014 – Nov 21, 2019Cancelled
Registration details
Analysis ID
5485d014f87d6ee251dcbc23aa30dc1e
License Form
Ministry of Health Medical Device Import No. 026681
Customs Code
DHA05602668106
Company information
Manufacturer Country
Viet Nam
Authorized Representative
OMRON HEALTHCARE TAIWAN CO., LTD.
Product details
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5630 Sprayer
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 21, 2014
Expiry Date
Nov 21, 2019
Cancellation Date
Jun 22, 2022
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 “OMRON” Compressor Nebulizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5485d014f87d6ee251dcbc23aa30dc1e and manufactured by OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD., and 1 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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