FDA Registration
Active
🇨🇳 China
CHANGSHA MAGILL MEDICAL TECHNOLOGY CO., LTD.
Reg #: 3021010418
·
FEI: 3021010418
·
Expires 2026
Products
4
Proprietary Names
9
Establishment Types
2
Classifications
4
Registration Details
- Registration Name
- CHANGSHA MAGILL MEDICAL TECHNOLOGY CO., LTD.
- Registration Number
- 3021010418
- FEI Number
- 3021010418
- Status
- Active
- Expiry Year
- 2026
- Initial Importer
- No
- Address
- Room 101-201, Bldg 1, No. 41, Yannong Road, Hi-Tech Development Zone
- City
- Changsha Hunan
- Country
- CN
Owner / Operator
- Firm Name
- Changsha Magill Medical Technology Co., Ltd.
- Operator Number
- 10082989
- Address
- Room 101-201, Bldg 1, No. 41, Yannong Road, Hi-Tech Development Zone
- City
- Changsha
- State
- Hunan
- Postal Code
- 410000
- Country
- CN
- Correspondent
- Hongjun Li
US Agent
- Business Name
- SHARE INFO INC.
- Contact Name
- Clare Ho
- Address
- 3557 158th St Flushing, NY
- City
- Flushing
- State
- NY
- ZIP
- 11358
- Country
- US
- [email protected]
- Phone
- 929 4102964
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | Class 1 | Anesthesiology | No | 2022-12-19 |
| Stylet, Tracheal Tube | BSR | Class 1 | Anesthesiology | No | 2022-12-19 |
| Airway, Oropharyngeal, Anesthesiology | CAE | Class 1 | Anesthesiology | No | 2021-10-19 |
| Laryngoscope, Non-Rigid | CAL | Class 1 | Anesthesiology | No | 2021-10-19 |
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)
Videoscope (Model: MGL-SP-C, MGL-SP-6)
Videoscope (Model: EM-16A, EM-16C, EM-64A, EM-64C)
Videoscope (Model: A8, B8)
Establishment Types
Manufacture Medical Device
Complaint File Establishment per 21 CFR 820.198