Joimax GmbH
DE-MF-000009201 · Germany · Karlsruhe
Joimax GmbH is registered in the European database on medical devices as a manufacturer, with 1 137 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 950 |
|---|---|
| Class IIb | 187 |
Among these devices, 324 are declared sterile, 167 implantable, 571 reusable, 55 active.
Devices declared under this manufacturer
- Biopsy Forceps, Blakesley
- Endo-Chisel, with handle
- Endo-Kerrison-Shaft
- EndoLIF® DoubleWedge-Cage 13 Short 12°
- Guiding Rod, conical with 2 excenter bores
- Guiding Rod, conical with center and excenter bore
- Olive Cutter, Olive Tip, with side protection
- Shrill® Deflector Shaft 2, WL= 320mm, reusable
- TESSYS® Guiding Rod, curved, green
- TESSYS® XT Extension Set Sterilization Tray
- Trial Implant Cages 11
- Working Tube for detachable handle
Showing 12 of 1 137 declared devices.
Catalogue references include ELDW64271312, ELO640011T, GRD205610, GRD226315, JSBOC274536, TEC273715.
European nomenclature codes declared: L1199, P090799, L110602, Z12130585, S010401, P09070101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | JOIMAX GMBH (DE) · FDA 3005083075 |
| Devices in EUDAMED | 1 137 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 1 137 |
|---|---|
| Found in the U.S. device database | 1 076 |
| Share | 94.6 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. Joimax GmbH is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G11 049319 0011 | issued | 2029-02-04 |
G10 049319 0007 | supplemented | 2029-01-31 |