POSTHORAX s.r.o.
SK-MF-000003610 · Slovakia · Bratislava
POSTHORAX s.r.o. is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 34 |
|---|
Most frequent device types declared: ICU Sternum Support Vest, Sternum Support Vest.
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- ChestFix Thoracic Elastic Tape
- POSTHORAX ICU Bra D
- POSTHORAX ICU Gentlemen M
- POSTHORAX ICU Ladies XL
- POSTHORAX PRO Gentlemen L
- POSTHORAX PRO Gentlemen M
- POSTHORAX PRO Gentlemen XL
- POSTHORAX PRO Gentlemen XXL
- POSTHORAX PRO Ladies L
- POSTHORAX PRO Support BRA B
- POSTHORAX PRO Support BRA D
- ThoraxBelt L
Showing 12 of 34 declared devices.
Catalogue references include 10.1203, 11.1202, 11.1203, 11.1205, 20.0204, 20.0210.
European nomenclature codes declared: M030599.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Posthorax Inc. (US) · FDA 3009067117 |
| Devices in EUDAMED | 34 |
| Country of registration | Slovakia |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 34 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.