Taiwan FDA registration f442ec45e114d7253f10a5adf6b867a7

"Leishi" double positive pressure respiratory system

TW: “磊仕”雙正壓呼吸系統
Taiwan flagTaiwan·Risk Class 2·RESPIRONICS INC.;; Respironics, Inc.·Registered Jan 12, 2018 – Jan 12, 2028Active
Registration details
Analysis ID
f442ec45e114d7253f10a5adf6b867a7
Customs Code
DHA05603070509
Company information
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 12, 2018
Expiry Date
Jan 12, 2028
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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 f442ec45e114d7253f10a5adf6b867a7 and manufactured by RESPIRONICS INC.;; Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including 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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