Taiwan FDA registration fe47ca8b4b19901751d639f7062ca44d

"Leishi" double positive pressure respiratory system

TW: “磊仕”雙正壓呼吸系統
Taiwan flagTaiwan·Risk Class 2·RESPIRONICS, INC.·Registered Mar 07, 2013 – Mar 07, 2028Active
Registration details
Analysis ID
fe47ca8b4b19901751d639f7062ca44d
Customs Code
DHA00602449101
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
Mar 07, 2013
Expiry Date
Mar 07, 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 fe47ca8b4b19901751d639f7062ca44d 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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