Taiwan FDA registration 582fc980d3b9d3aa09c6685b1bb01585

"Da Chung" Drug Delivery Device (Non-Sterile)

TW: "大中" 吸藥輔助器 (未滅菌)

Taiwan·Risk Class 1·MD·Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory·Registered May 12, 2017 – May 12, 2027Active

Registration details

Analysis ID: 582fc980d3b9d3aa09c6685b1bb01585
License Form: Ministry of Health Medical Device Manufacturing No. 006723

Company information

Manufacturer: Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Dazhong Medical Equipment Co., Ltd. Dongshan No. 2 Factory

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5640 Non-respiratory medical nebulizer
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 12, 2017
Expiry Date: May 12, 2027

About this record

Access comprehensive regulatory information for "Da Chung" Drug Delivery Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 582fc980d3b9d3aa09c6685b1bb01585 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.