Haemotronic S. p. A
IT-MF-000029734 · Italy · MIrandola
Haemotronic S. p. A is registered in the European database on medical devices as a manufacturer, with 22 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 22 |
|---|
Most frequent device types declared: Infusion therapies accessories, WASTE BAGS.
Among these devices, 16 are declared sterile.
Devices declared under this manufacturer
- AQUASAFE
- Aqua-Y
- Aqualine
- Aqualine RCA
- Aqualine S
- Aqualine S RCA
- Aquaspike 2
- Aquaspike-Y
- B 3052
- H4019
- NIK3188
- P41 V
Showing 12 of 22 declared devices.
Catalogue references include 1402104406, 1500074406, 1500094406, 1500194406, 1500994406, 1504015404.
European nomenclature codes declared: F020199, F020180, F90040101, F9080, A088099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 22 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 22 |
|---|---|
| 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. Haemotronic S. p. A was not found in either the U.S. or the Canadian register.