Data / Medical devices / Belgium / Dimequip
Dimequip: FDA-registered device maker in Frameries Hainaut, Belgium, 13 510(k) clearances
Dimequip is registered with the FDA (registration 3002808467) in Frameries Hainaut, Belgium. It lists 9 device types. The FDA files 13 510(k) clearances under its listings, the newest dated October 13, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3002808467
- Address
- Route de Bavay, Frameries Hainaut, Belgium, 7080
- Owner or operator
- VYGON S A (8020785)
- Roles
- Manufacturer
- First device listed
- November 21, 2006
- Registered through
- 2026
- Brand names listed
- 1361, 1362, 1363, 1364, 246X2, 339172, 361, 362 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass | DTL | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Intravascular, Diagnostic | DQO | 2 | Manufacturer | accessdata.fda.gov |
| Catheter, Umbilical Artery | FOS | 2 | Manufacturer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Manufacturer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Manufacturer | accessdata.fda.gov |
| Introducer, Catheter | DYB | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Manufacturer | accessdata.fda.gov |
| Tube, Feeding | FPD | 2 | Manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 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 |
|---|---|---|---|---|---|---|
| October 13, 2011 | K100163 | NUTRISAFE 2 FEEDING TUBES MODEL 362.XXX. 1362.XXX | FPD | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| September 15, 2006 | K060944 | NUTRISAFE 2 | FPD | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| March 23, 1998 | K974806 | VYGON NEO-SUMP | KNT | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| May 2, 1994 | K925854 | VYGON - ENTERAL FEEDING TUBE - POLYURETHANE | KNT | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| October 26, 1992 | K921374 | VYGON XRO VENOUS/ARTERIAL UMBILICAL CATHETER | FOS | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| May 20, 1991 | K910909 | MUCAID | BSY | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| February 11, 1986 | K860285 | XRO GASTRO-DUODENAL, DUAL FLOW TUBE, SALEM TYPE | KNT | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| July 15, 1985 | K851473 | VYGON DELEE SUCTION CATHETER CODE NO 533 | BSY | Substantially Equivalent | Vygon Corp. | accessdata.fda.gov |
| November 16, 1982 | K822879 | ENTERAL NUTRITION 1 | KNT | Substantially Equivalent | Exco, Inc. | accessdata.fda.gov |
| October 15, 1982 | K822836 | MICROFLEX-VENOFLUX | FPA | Substantially Equivalent | Exco, Inc. | accessdata.fda.gov |
| November 27, 1981 | K813143 | DESILET | DYB | Substantially Equivalent | Exco, Inc. | accessdata.fda.gov |
| November 27, 1981 | K813141 | VYGON STOPCOCKS & RAMPS(MANIFOLDS) | DTL | Substantially Equivalent | Exco, Inc. | accessdata.fda.gov |
| November 27, 1981 | K813140 | VYGON EXTENSION TUBES & CONNECTORS | DQO | Substantially Equivalent | Exco, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Umbilical Artery
- All makers of Catheter, Intravascular, Diagnostic
- All makers of Tubes, Gastrointestinal (And Accessories)
- All makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- All makers of Introducer, Catheter
- All makers of Set, Administration, Intravascular
Updated October 13, 2011. 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.