Cavex Holland BV
NL-MF-000000423 · Netherlands · Haarlem
Cavex Holland BV is registered in the European database on medical devices as a manufacturer, with 96 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 96 |
|---|
Most frequent device types declared: Cavex Alginate Impression Materials, Cavex Amalgam Alloys, Dental Impression Material, Silicone Rubber, Dental Impression Materials, other, Dental Wax.
Among these devices, 54 are declared implantable.
Devices declared under this manufacturer
- Cavex Bite&White Shade Correction HP25 Pen Bulk Pack
- Cavex Cream Alginate Fast Set 20x500g
- Cavex Individual Trays Lower Plain
- Cavex SiliconA Bite
- Cavex SiliconA Heavy Body
- Kulzer Vivida Office Pen 25% Refill
- Quadrant Anterior Shine capsule A2
- Quadrant Anterior Shine capsule A4
- Quadrant Anterior Shine capsule C4
- Quadrant Anterior Shine capsule D3
- Quadrant Flow syringe A3.5
- Quadrant Universal LC starterkit syringes
Showing 12 of 96 declared devices.
Catalogue references include 66100135, AA605, AS52, AS54, FA61, FA64T.
European nomenclature codes declared: Q01010103, Q010699, Q01010101, Q01020101, Q01010403, Q01010199.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | CAVEX HOLLAND B.V. (NL) · FDA 9614573 |
| Devices in EUDAMED | 96 |
| Country of registration | Netherlands |
⚠️ A similar name exists; we do not assert it is the same company — why.
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 1710455-1 | issued | 2026-10-15 |