Home › Device types › NZG
Bassinet, Hospital
FDA product code NZG · Class 2 · General Hospital
87
Registered devices
104
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
Pedigo Products, Inc. — PEDIGO PRODUCTS, INC.Amico Patient Care Corporation — Amico Patient Care CorporationUMF Medical — UNITED METAL FABRICATORS, INC.Pedigo Products, Inc. — PEDIGO PRODUCTS, INC.UMF Medical — UNITED METAL FABRICATORS, INC.Pedicraft — PEDICRAFT, INC.Pedicraft — PEDICRAFT, INC.Medviron Bassinet — MEDVIRON LLCBassinest Hospital Series — HALO INNOVATIONS, INC.Medviron — MEDVIRON LLCPedicraft — PEDICRAFT, INC.Pedigo Products, Inc. — PEDIGO PRODUCTS, INC.Well Baby Bassinet — DATEX-OHMEDA INCAmico Patient Care Corporation — Amico Patient Care CorporationTHE KERRI BEAR MATERNITY BASSINET — Imperial Surgical LtdPedigo Products, Inc. — PEDIGO PRODUCTS, INC.Bassinet — HILL-ROM, INC.Medviron Bassinet — MEDVIRON LLCWell Baby Bassinet — DATEX-OHMEDA INCWell Baby Bassinet — DATEX-OHMEDA INCMedviron — MEDVIRON LLCMedviron — MEDVIRON LLCPedigo Products, Inc. — PEDIGO PRODUCTS, INC.Couplet Care Bassinet — Couplet Care, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-10-10 | Stryker Medical Division of Stryker Corporation | It was identified that the volume of air inside the mattress may expand in regions of high altitude which may result in an unintended gap between the plateau of |
| 2011-10-14 | Nemschoff Chairs, Inc. | To correct issues with casters, door hinges, drawer slides, and the bassinet surround. Also, to add labeling to the product regarding specific instructions for |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
