Erba Lachema s.r.o.
CZ-MF-000024067 · Czechia · Brno
Erba Lachema s.r.o. is registered in the European database on medical devices as a manufacturer, with 113 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: CHEM-7, EC 90, ELite 580, H360, H560.
Devices declared under this manufacturer
- Erba H360 Dil
- Erba H560 Lyse1
- Erba H7 ret CON
- Erba H7100 Lyse 2 (500 mL)
- FE 125
- HDL/LDL CAL
- LDH 100
- LDH-L 250
- MG 250
- MP 100
- P AMY 100
- UA SINGLE 200
Showing 12 of 113 declared devices.
Catalogue references include BLT00037, BLT00039, BLT00045, BLT00067, HEM00031, HEM00059.
European nomenclature codes declared: W0103010105, W01010803, W0103010502, W01010230, W0103010503, W0103010501.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 113 |
| Country of registration | Czechia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 113 |
|---|---|
| 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.
North American profile: Neither register. Erba Lachema s.r.o. was not found in either the U.S. or the Canadian register.