Taiwan FDA registration ae20c4460ce4db16f8ba09b3989b3f46
“Seoil Pacific” Mechanical In-Exsufflator with Oscillation Vest
TW: “索爾派克” 咳痰輔助器及胸腔壁震動背心
Registration details
- Analysis ID
- ae20c4460ce4db16f8ba09b3989b3f46
- License Form
- Ministry of Health Medical Device Import No. 027238
- Customs Code
- DHA05602723807
Company information
- Manufacturer
- Seoil Pacific Corp.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- RTSYSTEM INC.
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
- Mar 27, 2015
- Expiry Date
- Mar 27, 2025
About this record
Access comprehensive regulatory information for “Seoil Pacific” Mechanical In-Exsufflator with Oscillation Vest in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae20c4460ce4db16f8ba09b3989b3f46 and manufactured by Seoil Pacific Corp.. The authorized representative in Taiwan is RTSYSTEM INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices