Tammer BioLab Oy
FI-MF-000010901 · Finland · Tampere
Tammer BioLab Oy is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: BBE, CAMS, CHOC+VIT, CHR-MRSA, CHR-URI.
Devices declared under this manufacturer
- Bacteroides bile esculin (BBE) agarmalja
- Campylobacter agarmalja (mCCDA)
- Columbia-malja hevosenverellä
- Fastidious anaerobe (FAA) agarmalja
- Kromogeeninen MRSA agarmalja
- Kromogeeninen Staph. aureus agarmalja [FI]
- Kromogeeninen agarmalja virtsaviljelyyn
- Lammasveriagar, selektiivinen malja
- Mueller-Hinton agar (MHA) herkkyysmalja
- S. aureus rikastusliuos, 7 ml kierrekorkillinen putki
- Seleniitti-kystiini liuos, 4 ml putki [FI]
- Suklaamalja vitamiinilisällä
Showing 12 of 36 declared devices.
Catalogue references include T007, T017, T019, T039, T047, T120.
European nomenclature codes declared: W0104010405, W0104010206, W0104010402, W0104030201, W0104010403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| Country of registration | Finland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 36 |
|---|---|
| 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. Tammer BioLab Oy was not found in either the U.S. or the Canadian register.