Data / Medical devices / Belgium / Pharmamed SA.
Pharmamed SA.: FDA-registered device maker in Anderlecht Brussels-Capital Region, Belgium, 7 510(k) clearances
Pharmamed SA. is registered with the FDA (registration 3037918935) in Anderlecht Brussels-Capital Region, Belgium. It lists 18 device types. The FDA files 7 510(k) clearances under its listings, the newest dated November 1, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3037918935
- Address
- Boulevard Sylvain Dupuis 280/3, Anderlecht Brussels-Capital Region, Belgium, 1070
- Owner or operator
- Pharmamed SA. (10093219)
- Roles
- Exporter to the US
- First device listed
- April 14, 2025
- Registered through
- 2026
- Brand names listed
- BANDAGE, ELASTIC, Bandage, liquid, CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE), Circuit, breathing (w connector, adaptor, y piece), Drape, surgical, exempt, Dressing, wound, drug, Dressing, wound, hydrophilic, Dressing, wound, occlusive and more
Devices it lists
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 1, 2024 | K242320 | BD Vacutainer® One Use Holder | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| July 27, 2015 | K151698 | BD Angiocath IV Catheter, BD Insyte IV Catheter | FOZ | Substantially Equivalent | Becton Dickinson Infusion Therapy Systems, Inc. | accessdata.fda.gov |
| July 14, 2015 | K150844 | Shiley Adult Flexible Tracheostomy Tube Cuffless, Reusable Inner Cannula, Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff, Reusable Inner Cannula | JOH | Substantially Equivalent | Covidien | accessdata.fda.gov |
| September 15, 2010 | K100029 | MEPILEX BORDER AG DRESSING | FRO | Substantially Equivalent | Molnlycke Health Care | accessdata.fda.gov |
| May 18, 2007 | K070964 | KLEENSPEC SINGLE USE VAGINAL SPECULUM AND 790 SERIES CORDLESS ILLUMINATION SYSTEM | HIB | Substantially Equivalent | Welch Allyn, Inc. | accessdata.fda.gov |
| October 1, 1999 | K992734 | BECTON DICKINSON SYRINGE | MEG | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| February 5, 1996 | K955103 | 3M NO STING BARRIER FILM | KMF | Substantially Equivalent | 3M Medical Products Group | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Antistick
- All makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- All makers of Otoscope
- All makers of Speculum, Vaginal, Nonmetal
- All makers of Bandage, Elastic
- All makers of Bandage, Liquid
Updated November 1, 2024. 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.