Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter
- Primary DI
- 10801741052306
- Brand
- Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter
- Company
- C. R. Bard, Inc.
- Model
- 0046120
- Catalog number
- 0046120
- Device description
- Bard® Nasogastric Sump Tube with PreVent® Anti-Reflux Filter
- Published
- 2016-08-16
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| FEG | TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| FEG | Tube, Double Lumen For Intestinal Decompression And/Or Intubation | Gastroenterology, Urology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 10801741052306 | Package | GS1 | 50 | In Commercial Distribution |
| 00801741052309 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 10801741052306 | 10801741052306 | | |
| 00801741052309 | 00801741052309 | 801741052309 | 0801741052309 |
GMDN Terms
| Term | Definition |
|---|
| Nasogastric feeding tube | A sterile, thin, flexible, hollow cylinder intended to access the stomach of a patient through the nose and nasopharynx primarily for enteral feeding and the administration of medications, either by gravity or with a pump; it may also be used for aspiration of gastric contents (e.g., gastric secretions). It is typically a single lumen, rubber or plastic tube of various diameters (typically smaller than those of nasogastric tubes intended primarily for decompression) with circular markings that serve as insertion guides. It is frequently used for very ill or comatose patients. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Length | 48 | Inch |
Regulatory Flags
- DUNS number
- 016898496
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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