NA
- Primary DI
- 30845854080744
- Brand
- NA
- Company
- Conmed Corporation
- Model
- RVFT10
- Catalog number
- RVFT10
- Device description
- Fluid trap
- Published
- 2020-06-06
- 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
- false
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| GAZ | TUBING, NONINVASIVE |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| GAZ | Tubing, Noninvasive | General Hospital | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 30845854080744 | Package | GS1 | 10 | In Commercial Distribution |
| 10815198011724 | Previous | GS1 | 0 | |
| 20845854080747 | Primary | GS1 | 0 | |
| 00845854080743 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 30845854080744 | 30845854080744 | ||
| 10815198011724 | 10815198011724 | ||
| 20845854080747 | 20845854080747 | ||
| 00845854080743 | 00845854080743 | 845854080743 | 0845854080743 |
GMDN Terms
| Term | Definition |
|---|---|
| Surgical plume evacuation system filter | A screening device designed for use with a surgical smoke evacuation system, to entrap particulates from the plume of smoke created typically through the use of various tissue-burning surgical devices (e.g., laser, electrosurgical diathermy device), to prevent this from exhausting into the ambient air or evacuation tubing/pipeline systems. It will typically have a hydrophobic membrane that retains the particulate/bacterial pathogens through a combination of mechanical, electrostatic, or other means. The device comes in various sizes and designs. This is a reusable device, typically with a limited lifetime (e.g., 5 hours, 20 procedures, or weekly exchange). |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)237-0169 | CUSTOMER_SERVICE@CONMED.COM |
Regulatory Flags
- DUNS number
- 071595540
- Device count
- 10
- 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
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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