Data / Medical devices / Saudi Arabia / Alshifa Medical Products Co. (CJS)
Alshifa Medical Products Co. (CJS): FDA-registered device maker in Damman, Eastern Province Ash Sharqiyah, Saudi Arabia, 2 510(k) clearances
Alshifa Medical Products Co. (CJS) is registered with the FDA (registration 9680597) in Damman, Eastern Province Ash Sharqiyah, Saudi Arabia. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated July 25, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9680597
- FEI number
- 3003767808
- Address
- 1ST INDUSTRIAL CITY Road 22, Cross 11, Damman, Eastern Province Ash Sharqiyah, Saudi Arabia, 31472
- Owner or operator
- ALSHIFA MEDICAL PRODUCTS CO. (CJS) (9010052)
- Roles
- Manufacturer
- First device listed
- July 15, 2008
- Registered through
- 2026
- Brand names listed
- RAMY HYPODERMIC SYRINGE, RAMY HYPODERMIC SYRINGE WITH NEEDLE, Ramy Hypodermic 1 ml TUBERCULIN, Ramy Hypodermic Syringe 10 ml Eccentric Tip, Ramy Hypodermic Syringe 10 ml Luer Lock Tip, Ramy Hypodermic Syringe 10 ml Luer Slip Tip, Ramy Hypodermic Syringe 20 ml Eccentric Tip, Ramy Hypodermic Syringe 20 ml Luer Lock Tip and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Syringe, Piston | FMF | 2 | 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 |
|---|---|---|---|---|---|---|
| July 25, 1997 | K971664 | RAMY PISTON SYRINGE | FMF | Substantially Equivalent | Alshifa Medical Syringes Mfg. Co., Ltd. | accessdata.fda.gov |
| July 24, 1997 | K972452 | RAMY INTEGRATED NEEDLE SYRINGE | FMF | Substantially Equivalent | Alshifa Medical Syringes Mfg. Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 25, 1997. 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.