Pharmico Medical Korlátolt felelősségi társaság - MF
HU-MF-000018352 · Hungary · Debrecen,
Pharmico Medical Korlátolt felelősségi társaság - MF is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 33 |
|---|
Most frequent device types declared: IALUADATER/UroDapter, Műtéti szett, Pharmico Műtéti Szett, Pharmico Műtéti szett.
Among these devices, 33 are declared sterile.
Devices declared under this manufacturer
- A-Tex Tracheal kompresse 13 x 9cm
- IALUADAPTER/UroDapter
- Pharmico Bütykös szett
- Pharmico Fül-Orr-Gége III
- Pharmico Fül-Orr-Gége IV
- Pharmico Fül-Orr-Gége VI
- Pharmico Szemészet I
- Pharmico Szívsebészet Gyerek
- Pharmico Szülészet-Nőgyógyászat I
- Pharmico Általános Sebészet I
- Pharmico Általános Sebészet III
- SEIDEL A-Tex Tracheal kompresse 7,5 x7,5 cm
Showing 12 of 33 declared devices.
Catalogue references include AB-5710, www.discountmed.hu, www.dispomedicor.hu, www.urosystem.hu.
European nomenclature codes declared: M0201020201, M030102, R040201, M0201020101, U0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 33 |
| Country of registration | Hungary |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 33 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 3.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Pharmico Medical Korlátolt felelősségi társaság - MF was not found in either the U.S. or the Canadian register.