Ri Mos. S.R.L.
Ri Mos. S.R.L. holds FDA 510(k) medical device clearances, cleared in 1999.
Top product codes for Ri Mos. S.R.L.
Recent clearances by Ri Mos. S.R.L.
- K992926 — GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195)
- K991895 — RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217)
- K991827 — GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043
- K983897 — CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G
Data sourced from openFDA. This site is unofficial and independent of the FDA.