Rand S.R.L.
Rand S.R.L. holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2016, with 2 FDA device recalls on record.
Top product codes for Rand S.R.L.
FDA recalls by Rand S.R.L.
- Z-2048-2021 — Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120
- Z-2049-2021 — Ch24 round silicone catheter, Diameter: 8 mm, Perforated section: 230 mm, Total length: 600 mm, Reference Code R9900099. Thoracic/abdominal cavity drain catheter.
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 Rand S.R.L.
Data sourced from openFDA. This site is unofficial and independent of the FDA.