Xeridiem Medical Devices, Inc.
14 product lines across 1 device categories: G-tubes.
About Xeridiem Medical Devices, Inc.
Xeridiem Medical Devices, Inc. hasn't added a company description yet.
Gastrostomy and GJ Tubes
Used in: Gastrostomy (G-Tube) Placement, Gastrojejunostomy (GJ-Tube) Placement
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Entuit Thrive LP | Catheter Gauge: 12β24 Fr; Length: 0.8β5 cm | 64 | Not stated |
| EndoVive | Catheter Gauge: 12β28 Fr | 16 | Not stated |
| Gastrostomy Feeding Tube with ENFit Connector Gastrostomy Feeding Tube with ENFit Connector 12FR | Catheter Gauge: 12β24 Fr | 7 | MR Conditional |
| EndoVive Gastrostomy Tube, Right Angle, with ENFit Connector EndoVive Gastrostomy Tube, Right Angle, with ENFit Connector, 22FR | Catheter Gauge: 12β24 Fr | 7 | MR Conditional |
| Entuit Thrive Entuit Gastrostomy BR Balloon Retention Feeding Tube, 22 FR Ref. Number: SBRD-22 | Catheter Gauge: 12β24 Fr | 7 | Not stated |
| Entuit Gastrostomy BR Balloon Retention Feeding Tube with ENFit Connection Entuit Gastrostomy BR Balloon Retention Feeding Tube with ENFit Connection, 20 FR | Catheter Gauge: 12β24 Fr | 7 | MR Conditional |
| EndoVive Gastrostomy Tube, Straight, with ENFit Connector EndoVive Gastrostomy Tube, Straight, with ENFit Connector, 14 FR | Catheter Gauge: 12β24 Fr | 7 | MR Conditional |
| Vesco 14 Fr - Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) | Catheter Gauge: 14β24 Fr | 6 | MR Conditional |
| Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) Gastrostomy Tube - Dual ENFit Port (Tri-Funnel) 18FR | Catheter Gauge: 14β24 Fr | 6 | MR Conditional |
| ENFit Feeding Port Transition Connector | β | 1 | Not stated |
| Kangaroo 12" Bolus Feed Extension Set with ENFit Connector | β | 1 | Not stated |
| Kangaroo Skin Level Device 12FR x 0.80cm | Catheter Gauge: 12 Fr; Length: 80 cm | 1 | Not stated |
| Kangaroo 24" Continuous Feed Extension Set with ENFit Connector | β | 1 | Not stated |
| Kangaroo Skin Level Device Kit Extension Sets | β | 1 | Not stated |
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Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.