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“Respironics” Dorma Auto-CPAP Device - Taiwan Registration 737851d2d1648626c3eea4a91d9951aa

Access comprehensive regulatory information for “Respironics” Dorma Auto-CPAP Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 737851d2d1648626c3eea4a91d9951aa and manufactured by Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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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737851d2d1648626c3eea4a91d9951aa
Registration Details
Taiwan FDA Registration: 737851d2d1648626c3eea4a91d9951aa
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Device Details

“Respironics” Dorma Auto-CPAP Device
TW: “磊仕”陽壓呼吸器
Risk Class 2
MD

Registration Details

737851d2d1648626c3eea4a91d9951aa

Ministry of Health Medical Device Import No. 030434

DHA05603043404

Company Information

United States

Product Details

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

D Devices for anesthesiology

D5905 Discontinuous respirators

Imported from abroad

Dates and Status

Nov 20, 2017

Nov 20, 2022