Taiwan FDA registration d4dc133d53887597c360303b36e35bd1
"Leishi" Newnes gel mask
TW: “磊仕”紐恩斯凝膠面罩
Registration details
- Analysis ID
- d4dc133d53887597c360303b36e35bd1
- Customs Code
- DHA09200059106
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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Jun 05, 2014
- Expiry Date
- Jun 05, 2024
About this record
Access comprehensive regulatory information for "Leishi" Newnes gel mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d4dc133d53887597c360303b36e35bd1 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