Taiwan FDA registration 42028a18a40ce42e3d4f723af833ac70

"Respironics" Nasal oxygen catheter (Non-Sterile)

TW: "磊仕" 經鼻氧氣導管 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NEXTPHASE MEDICAL DEVICES MEXICO LLC·Registered Dec 02, 2020 – Dec 02, 2025Expired
Registration details
Analysis ID
42028a18a40ce42e3d4f723af833ac70
License Form
Ministry of Health Medical Device Import No. 022149
Customs Code
DHA09402214903
Company information
Manufacturer Country
Mexico
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Transnasal Oxygen Catheter (D.5350)".
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5350 Nasal oxygen catheter
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 02, 2020
Expiry Date
Dec 02, 2025
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About this record

Access comprehensive regulatory information for "Respironics" Nasal oxygen catheter (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42028a18a40ce42e3d4f723af833ac70 and manufactured by NEXTPHASE MEDICAL DEVICES MEXICO LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VOLCANO CORPORATION BY VOLCARICA S.R.L., and 1 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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