FDA device listing
MiniCap with Povidone-Iodine Solution
FDA device listing 1853369401 · Vantive US Healthcare LLC
Key facts
| Proprietary names | MiniCap with Povidone-Iodine Solution |
|---|---|
| Owner/operator | Vantive US Healthcare LLC |
| Owner/operator number | 9038727 |
| Premarket submissions | K152129 |
| Product codes | KDJ |
| Device names | KDJ - Set, Administration, For Peritoneal Dialysis, Disposable |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5630 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | BAXTER S.A. DE C.V., Gambro UF Solutions LLC, Vantive Manufacturing Limited, Vantive US Healthcare LLC |
| Establishment registrations | 8030639, 9612168, 3003504604, 3038195011 |
| FEI numbers | 6898, 3002806471, 3003504604, 3038195011 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database