Techno-path Manufacturing Ltd.
IE-MF-000001822 · Ireland · Co. Tipperary
Techno-path Manufacturing Ltd. is registered in the European database on medical devices as a manufacturer, with 207 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: CVG100P, CVG200B, CVG300P, CVN100N, CVN200N.
Devices declared under this manufacturer
- Lp-PLA2 Calibrator
- Multichem AE
- Multichem CSF
- Multichem IA
- Multichem IA Plus
- Multichem IA Speciality
- Multichem ID-COVID19 G
- Multichem MS Free TDMs
- Multichem MS Steroids
- Multichem MS TDMs
- Multichem MS VItD
- Multichem S Plus
Showing 12 of 207 declared devices.
Catalogue references include 06S7801, 08P89-10, 09922512190, AE600A, BP302X, CH100MCRP.
European nomenclature codes declared: W0101050101, W0102152099, W0101050102, W0102152002, W0101050208, W0102050215.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | TECHNO-PATH MANUFACTURING LTD. (IE) · FDA 3008156187 |
| Devices in EUDAMED | 207 |
| Country of registration | Ireland |
Device-level evidence
| Devices with a numeric GTIN | 207 |
|---|---|
| Found in the U.S. device database | 181 |
| Share | 87.4 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | TECHNO-PATH MANUFACTURING LTD. |
What it holds in Canada
| Licences on record | 12 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 7 |
| Class 3 devices | 5 |
| First licensed | 2013-11-14 |
Licence types: Device Family (8), Test Kit (2), Single Device (2).
Licensed under: TECHNO-PATH MULTICHEM IA/IA PLUS, TECHNOPATH MULTICHEM, TECHNOPATH MULTI-CHECK COMBI, TECHNOPATH MULTICHEM, MULTICHEM IA PLUS, MULTICHEM MS VITD.
North American profile: Both markets. Techno-path Manufacturing Ltd. is registered in both the United States and Canada.