Zhongshan Wesee Meditech Co., Ltd.
Registered establishment in Zhongshan, Guangdong, China. 3 device types.
Zhongshan Wesee Meditech Co., Ltd. is a contract manufacturer holding a current FDA establishment registration. The registration covers Laryngoscope, Rigid, Laryngoscope, Non-Rigid and 1 other device type. Its earliest product listing with the FDA dates from 2023.
Registration
| Registered name | ZHONGSHAN WESEE MEDITECH CO., LTD. |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3027655341 |
| FEI number | 3027655341 |
| Establishment type | Contract manufacturer, Manufacturer |
Chinese Registration
| Chinese legal name | 中山市微视医用科技有限公司 |
|---|---|
| Unified social credit code | 91442000MA554N3A6J |
| Source | export sales certificate, Guangdong medical products administration |
Location
| City | Zhongshan |
|---|---|
| Province | Guangdong |
| Address | 4F/6F, Building C, No.2 Jianshuo Street, South China Modern Chinese Medicine Park, |
| Postal code | 528451 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Accessories, Photographic, For Endoscope (Exclude Light Sources) | Class 1 | Endoscopic Video Processor (M110A) | 2023 | 8 |
| Laryngoscope, Non-Rigid | Class 1 | Flexible laryngoscope(DP11A) | 2023 | 12 |
| Laryngoscope, Rigid | Class 1 | Disposable Video Laryngoscope(Q202D) | 2024 | 44 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2020 |
|---|---|
| Main products | Endoscope ENT, Endoscope Urology, Endoscope Pulmonary, Video processor |
| Certifications | ISO 13485, CE, ANVISA, TFDA, EU MDR, FDA |
| Export markets | Brazil, Thailand, Italy, Indonesia, EU, USA |
Nearby Manufacturers
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.
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