FDA Registration
Active
🇨🇳 China
EndoScreener
Reg #: 3016591389
·
FEI: 3016591389
·
Expires 2025
Products
1
Proprietary Names
1
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- CHENGDU WISION MEDICAL DEVICE CO., LTD.
- Registration Number
- 3016591389
- FEI Number
- 3016591389
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- Unit 802, Floor 8, Building 17, Yintaicheng, No.1999 Yizhou Road, Wuhou District
- City
- Chengdu Sichuan
- Country
- CN
Regulatory Submissions
- 510(k) Number
- K211326
Owner / Operator
- Firm Name
- Chengdu Wision Medical Device Co., Ltd.
- Operator Number
- 10084846
- Address
- Unit 802, Floor 8, Building 17, Yintaicheng, No.1999 Yizhou Road, Wuhou District
- City
- Chengdu
- State
- Sichuan
- Postal Code
- 610041
- Country
- CN
- Correspondent
- Jiong He
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Gastrointesinal Lesion Software Detection System | QNP | Class 2 | Gastroenterology, Urology | No | 2022-04-06 |
Proprietary Names
EndoScreener
Establishment Types
Manufacture Medical Device