Taiwan FDA registration e3616c0fdebd094048d587e3cde16426
"Leishi" slim nose mask
TW: “磊仕”纖細鼻面罩
Registration details
- Analysis ID
- e3616c0fdebd094048d587e3cde16426
- Customs Code
- DHA09200054206
Company information
- Manufacturer Country
- United States;;China
- 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 Anesthesiology
- Product Type (Level 2)
- D.5905 Non-continuous respirators
- Import Information
- Input;; Chinese goods;; Contract manufacturing
Dates and status
- Registration Date
- Aug 26, 2013
- Expiry Date
- Aug 26, 2028
About this record
Access comprehensive regulatory information for "Leishi" slim nose mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3616c0fdebd094048d587e3cde16426 and manufactured by RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices