AVID TruCustom
- Primary DI
- 20809160196899
- Brand
- AVID TruCustom
- Company
- AVID MEDICAL, INC.
- Model
- LANC028-22_0001
- Catalog number
- LANC028-22
- Published
- 2018-06-11
- 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 |
|---|
| OEZ | Cardiovascular procedure kit |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| OEZ | Cardiovascular Procedure Kit | Cardiovascular | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 20809160196899 | Package | GS1 | 2 | In Commercial Distribution |
| 10809160196892 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|
| 20809160196899 | 20809160196899 |
| 10809160196892 | 10809160196892 |
GMDN Terms
| Term | Definition |
|---|
| Arterial/central venous catheterization support/maintenance kit | A collection of sterile devices intended to support the catheterization procedure of an artery and/or central vein (large veins of the upper body), and/or to provide ongoing vascular catheter maintenance. It is primarily intended to be used at the patient’s bedside and includes devices intended to support catheter placement and/or or ongoing maintenance (e.g., dressing change, catheter flushing) such as: disposable drapes, disinfectant wipes, dressings, gown, tourniquets, ultrasound system transducer cover, coupling gel, sharps container, syringe, and saline solution; neither the catheter, catheter introduction device, nor pharmaceuticals are included. This is a single-use device. |
Regulatory Flags
- DUNS number
- 015623119
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- true
- HCT/P
- false
- Kit
- true
- 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
- true
- Sterilization required before use
- true
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