Primus Corporation Dba Trinity Biotech
Primus Corporation Dba Trinity Biotech holds FDA 510(k) medical device clearance, cleared in 2011, with 2 FDA device recalls on record.
Top product codes for Primus Corporation Dba Trinity Biotech
FDA recalls by Primus Corporation Dba Trinity Biotech
- Z-0349-2023 — A. MENARINI diagnostics Hb 9210 PREMIER, LEVEL1, LEVEL II, Hemoglobin A1c Controls for hemoglobin A1c Assay, REF 45052, part number 05-01-0926, A1c analysis
- Z-0350-2023 — Trinity Biotech HbA1c (GHb) Contorls Kit, 500uL (Levels I & II), REF 01-04-0020, Part number 05-01-0040B, A1c analysis
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Primus Corporation Dba Trinity Biotech
Data sourced from openFDA. This site is unofficial and independent of the FDA.