Data / Medical devices / China / Shanghai Medrise Industry Co., Ltd.
Shanghai Medrise Industry Co., Ltd.: FDA-registered device maker in Shanghai, China, 1 510(k) clearance
Shanghai Medrise Industry Co., Ltd. is registered with the FDA (registration 3021167963) in Shanghai, China. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 12, 2020. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3021167963
- Address
- RM A315, No.507, Changqing RD., Pudong New Area, Shanghai, China, 200126
- Owner or operator
- Shanghai MedRise Industry Co., Ltd. (10084334)
- Roles
- Exporter to the US
- First device listed
- February 10, 2022
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Exporter to the US | accessdata.fda.gov |
| Bedpan | FOB | 1 | Exporter to the US | accessdata.fda.gov |
| Chair, Adjustable, Mechanical | INN | 1 | Exporter to the US | accessdata.fda.gov |
| Container, Sharps | MMK | 2 | Exporter to the US | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Exporter to the US | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Exporter to the US | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 12, 2020 | K201523 | Sharps container | MMK | Substantially Equivalent | Zhejiang Gongdong Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Container, Sharps
- All makers of Bedpan
- All makers of Dispenser, Solid Medication
- All makers of Dispenser, Liquid Medication
- All makers of Adaptor, Hygiene
- All makers of Chair, Adjustable, Mechanical
Updated November 12, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.