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“Airsonett” Medical Mobile Air Cleaner - Taiwan Registration 668f3437755774beaa7f813759e1411c

Access comprehensive regulatory information for “Airsonett” Medical Mobile Air Cleaner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 668f3437755774beaa7f813759e1411c and manufactured by Airsonett, AB. The authorized representative in Taiwan is REVO LASER 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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668f3437755774beaa7f813759e1411c
Registration Details
Taiwan FDA Registration: 668f3437755774beaa7f813759e1411c
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Device Details

“Airsonett” Medical Mobile Air Cleaner
TW: “艾爾索尼”醫療專用空氣清淨儀
Risk Class 2
MD
Cancelled

Registration Details

668f3437755774beaa7f813759e1411c

Ministry of Health Medical Device Import No. 027162

DHA05602716200

Company Information

Sweden

Product Details

J General hospital and personal use equipment

J5045 Medical Recirculation Air Purifier

Imported from abroad

Dates and Status

Apr 20, 2015

Apr 20, 2020

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期