Oxygen Tubing Swivel Connector, bulk
- Primary DI
- 00709078002557
- Brand
- Oxygen Tubing Swivel Connector, bulk
- Company
- WESTMED, INC.
- Model
- 0590B
- Device description
- Oxygen Tubing Swivel Connector, bulk (This is a component of the Composite Kit for Performance Home Med - Part #0836)
- Published
- 2017-04-20
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes
| Code | Name |
|---|
| BYX | Tubing, Pressure And Accessories |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| BYX | Tubing, Pressure And Accessories | Anesthesiology | 1 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00709078002557 | Primary | GS1 | 0 | |
Alternate GTIN/UPC/EAN values are derived from GS1 digit structure for lookup convenience. Do not treat derived UPC-A or EAN-13 values as separate FDA identifiers. GTIN-14 values with indicator digits 1-9 usually represent packaging levels, cases, pallets, or variable-measure items and are not converted to UPC-A/EAN-13 here.
Alternate GTIN / UPC / EAN Codes
| Source identifier | Source length | GTIN-14 normalized | Indicator | UPC-A | EAN-13 | Conversion note |
|---|
| 00709078002557 | 14 | 00709078002557 | 0 | 709078002557 | 0709078002557 | Indicator 0 and prefix 00 allow UPC-A and EAN-13 conversion. |
GMDN Terms
| Term | Definition |
|---|
| Oxygen administration tubing | A length of flexible tube, typically a small bore, thick-walled, anti-kink tubing (to prevent blockage) intended for the delivery of a pure oxygen (O2) or an O2 enriched gas to a mask or nasal cannula, typically during delivery of dry O2 to the patient. The tubing is typically available in standard coil lengths and is cut by clinical staff to appropriate lengths to create an extension or connecting piece. This is a single-use device. |
Regulatory Flags
- DUNS number
- 092673953
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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