Taiwan FDA registration 737851d2d1648626c3eea4a91d9951aa
“Respironics” Dorma Auto-CPAP Device
TW: “磊仕”陽壓呼吸器
Taiwan·Risk Class 2·MD·Respironics, Inc.·Registered Nov 20, 2017 – Nov 20, 2022ExpiredRegistration details
- Analysis ID
- 737851d2d1648626c3eea4a91d9951aa
- License Form
- Ministry of Health Medical Device Import No. 030434
- Customs Code
- DHA05603043404
Company information
- Manufacturer
- Respironics, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5905 Discontinuous respirators
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 20, 2017
- Expiry Date
- Nov 20, 2022
About this record
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.
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