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“Da Chung” Humidification Chamber - Taiwan Registration db25ec0257153909745b4f07c3814f62

Access comprehensive regulatory information for “Da Chung” Humidification Chamber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db25ec0257153909745b4f07c3814f62 and manufactured by Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory. The authorized representative in Taiwan is Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory.

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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db25ec0257153909745b4f07c3814f62
Registration Details
Taiwan FDA Registration: db25ec0257153909745b4f07c3814f62
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Device Details

“Da Chung” Humidification Chamber
TW: “大中”加溫加濕瓶
Risk Class 2
MD

Registration Details

db25ec0257153909745b4f07c3814f62

Ministry of Health Medical Device Manufacturing No. 005764

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5450 Gas humidifier for respirators

Produced in Taiwan, China

Dates and Status

May 18, 2017

May 18, 2027