Ri Mos. S.r.l.
Country not established
- Devices
- 4
What Ri Mos. S.r.l. makes
Ri Mos. S.R.L. manufactures single-port and wedge-shaped RAMPIPELLA catheters for medical procedures, as well as a GINRAM endocervical single-oval port. Their portfolio includes cervical and contra-cervical anesthesia needles in 30-gauge lengths (4mm and 6mm) and various speculum designs, such as GINRAM SPECUVAG, GINRAM SPECUVAG AS, and GINRAM CUSCOVAG.
These devices fall under Class II regulatory classification in the US and are listed in the FDA’s 510(k) premarket notification registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Ginram Specuvag, Ginram Specuvag As, Ginram Cuscovag, Models 720101, 720102, 720103, 720179, 720227, 720043 Ref K991827
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ri Mos. S.R.L. have in the registry?
The registry currently lists 4 devices for Ri Mos. S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ri Mos. S.R.L.'s devices?
Among its 4 most recently registered devices, Ri Mos. S.R.L. has devices listed in FDA 510(k) (4 devices).
What risk classes do Ri Mos. S.R.L.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Ri Mos. S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ri Mos. S.R.L. in the registry?
The most recently registered devices listed for Ri Mos. S.R.L. include RAMPIPELLA, SINGE PORT (720196) & WEDGE-SHAPED PORT (720217), GINRAM ENDOCIC SINGLE OVAL PORT (MODEL NO. 720195), CERVICAL ANESTHESIA NEEDLE, CONTRACERVICAL ANESTHESIA NEEDLE, MODEL #'S 720209 30GAU X 4 MM, 720210 30GAU X 6MM, 720208G and GINRAM SPECUVAG, GINRAM SPECUVAG AS, GINRAM CUSCOVAG, MODELS 720101, 720102, 720103, 720179, 720227, 720043.