Data / Medical devices / China / MDF Instruments Medifriend Inc.
MDF Instruments Medifriend Inc.: FDA-registered device maker in Song Jiang District, Shanghai, China, 1 510(k) clearance
MDF Instruments Medifriend Inc. is registered with the FDA (registration 9680874) in Song Jiang District, Shanghai, China. It lists 13 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 14, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9680874
- FEI number
- 3000953362
- Address
- 1898 Lai Yin RD, BLDG 6, 3F / BLDG 2, 1F Jiu Ting Town, Song Jiang District, Shanghai, China, 201615
- Owner or operator
- MDF Instruments Medifriend Inc. (9012076)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- December 12, 1994
- Registered through
- 2026
- Brand names listed
- , PERCUSSOR, ASTIC SURGERY, BATTERY POWERED GENERAL HOSPITAL, EXAMINATION, FOR ENDOSCOPE, LIGHT, MANUAL CARDIOVASCULAR, MDF® Calibra Pro Aneroid Sphygmomanometer and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Manufacturer | accessdata.fda.gov |
| Bulb, Inflation, For Endoscope | FCY | 1 | Manufacturer | accessdata.fda.gov |
| Chart, Visual Acuity | HOX | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Manufacturer | accessdata.fda.gov |
| Fork, Tuning | GWX | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Instrument, Surgical, Disposable | KDC | 1 | Manufacturer | accessdata.fda.gov |
| Light, Examination, Medical, Battery Powered | KYT | 1 | Manufacturer | accessdata.fda.gov |
| Percussor | GWZ | 1 | Manufacturer | accessdata.fda.gov |
| Screw, Oral | KBW | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope Head | BZS | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Manufacturer | accessdata.fda.gov |
| Tape, Measuring, Rulers And Calipers | FTY | 1 | Manufacturer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 14, 1995 | K950778 | MEDIFRIEND PROFESSIONAL SPHYGMOMANOMETER | DXQ | Substantially Equivalent | Shanghai Medifriend Medical Products Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stethoscope, Manual
- All makers of Instrument, Surgical, Disposable
- All makers of Blood Pressure Cuff
- All makers of Light, Examination, Medical, Battery Powered
- All makers of Fork, Tuning
- All makers of Stethoscope Head
Updated March 14, 1995. 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.