Latvia MGI Tech
LV-MF-000017790 · Latvia · Marupes pagasts
Latvia MGI Tech is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: DNBSEQ-G400, DNBSEQ-G99, DNBSEQ-G99A.
Devices declared under this manufacturer
- Genetic Sequencer DNBSEQ-G400
- Genetic Sequencer DNBSEQ-G99
- Genetic Sequencer DNBSEQ-G99A
- Universal Sequencing Reaction Kit G99 SM App-D FCL PE150
- Universal Sequencing Reaction Kit G99 SM App-D FCL SE100
- Universal Sequencing Reaction Kit G99 SM App-D FCU PE150
- Universal Sequencing Reaction Kit G99 SM App-D FCU SE100
- Universal Sequencing Reaction Kit G99 SM FCL PE150
- Universal Sequencing Reaction Kit G99 SM FCL SE100/PE50
Catalogue references include 900-000492-00, 900-000612-00, 900-000628-00, 940-000431-00, 940-000434-00, 940-000525-00.
European nomenclature codes declared: W010699, W02050108.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Latvia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Latvia MGI Tech was not found in either the U.S. or the Canadian register.