CHANGSHA MAGILL MEDICAL TECHNOLOGY CO., LTD.

FDA Device Registration & Listing · Changsha Hunan, CN · Registration 3021010418

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3021010418
FEI Number
3021010418
Entity Name
CHANGSHA MAGILL MEDICAL TECHNOLOGY CO., LTD.
City/State/Country
Changsha Hunan, CN
Establishment Address
Room 101-201, Bldg 1, No. 41, Yannong Road, Hi-Tech Development Zone, Changsha Hunan 410000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Changsha Magill Medical Technology Co., Ltd. (Owner Number: 10082989)
Owner / Operator Contact Address
Room 101-201, Bldg 1, No. 41, Yannong Road, Hi-Tech Development Zone, Changsha, CN-HN 410000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Disposable laryngeal mask connector (Model: TRI-1) Disposable laryngeal mask connector (Model: TRI-2) Endotreacheal Tube Ejection Bar (Model: EJT-1) Disposable Video Laryngeal Mask (Model: Bronch#2, Bronch#2.5) Disposable Video Laryngeal Mask (Model: FlexiView #2, FlexiView #2.5, FlexiView #3, FlexiView #4, FlexiView #5) Disposable Video Laryngeal Mask (Model: Bronch#3, Bronch#4, Bronch#5)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece) Anesthesiology Class 1 868.5240 2022-12-19
BSR Stylet, Tracheal Tube Anesthesiology Class 1 868.5790 2022-12-19
CAE Airway, Oropharyngeal, Anesthesiology Anesthesiology Class 1 868.5110 2021-10-19

Official Correspondent

Hongjun Li

US Agent Details

Clare Ho Business: SHARE INFO INC. Email: cfrhealthcare@foxmail.com Phone: (929) 4102964

Related Public Records

Same Entity

Changsha Magill Medical Technology Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0033-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube with Bird adapter, oxygen supply tubing, sideport connector with adjustable bleed valve, and 40 cm H2O Popoff elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83124-2
Z-0034-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, ported elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83100-24
Z-0035-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, 40 cm H2O Popoff elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83144-24
Z-0036-04 VIASYS Med Systems 1
Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120
Z-0037-04 VIASYS Med Systems 1
Sideport Kit, consisting of an adjustable sideport valve and an O2 port elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83166

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021010418. Last updated year: 2026. Please use registration number 3021010418 when referencing this establishment in official correspondence.
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