Taiwan FDA registration d753927163dad1ecc60d9b35b6e3b1bb

"Leishi" double positive pressure respiratory system

TW: “磊仕”雙正壓呼吸系統
Taiwan flagTaiwan·Risk Class 2·Respironics, Inc.·Registered Jan 13, 2016 – Jan 13, 2026Expired
Registration details
Analysis ID
d753927163dad1ecc60d9b35b6e3b1bb
Customs Code
DHA05602814301
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 Anesthesiology
Product Type (Level 2)
D.5905 Non-continuous respirators
Import Information
import
Dates and status
Registration Date
Jan 13, 2016
Expiry Date
Jan 13, 2026
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About this record

Access comprehensive regulatory information for "Leishi" double positive pressure respiratory system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d753927163dad1ecc60d9b35b6e3b1bb and manufactured by Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including RESPIRONICS INC., RESPIRONICS INC.;; Respironics, Inc., and 5 recent registrations in the same category. 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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