FlexCath Advance™
- Primary DI
- 00643169688872
- Brand
- FlexCath Advance™
- Company
- MEDTRONIC, INC.
- Model
- 4FC12
- Device description
- SHEATH 4FC12 FLEXCATH ADVANCE 12F US
- Published
- 2016-08-11
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DRA | CATHETER, STEERABLE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DRA | Catheter, Steerable | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K123591 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00643169688872 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00643169688872 | 00643169688872 | 643169688872 | 0643169688872 |
GMDN Terms#
| Term | Definition |
|---|---|
| Haemostasis valve | A noninvasive device designed as a conduit through which a small-diameter diagnostic/interventional device(s) can be introduced into or withdrawn from a patient's vasculature while preventing backflow of blood; it might in addition be intended for urinary applications. It is intended to be attached, typically via Luer-lock, to an invasively-placed catheter introducer (not included) and typically has a self-sealing lumen(s) [e.g., Touhy-Borst valve] and sideport for the introduction of solutions. It may include noninvasive guidewire accessories (e.g., guidewire introducer). It is not designed to be connected between tubing (i.e., not an in-line valve). This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Length | 65 | Centimeter |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Handling Environment Humidity | 0 Percent (%) Relative Humidity | 85 Percent (%) Relative Humidity | |
| Handling Environment Temperature | -31 Degrees Fahrenheit | 136 Degrees Fahrenheit | |
| Special Storage Condition, Specify | 0 | 0 | Keep Dry |
| Storage Environment Temperature | 59 Degrees Fahrenheit | 86 Degrees Fahrenheit |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)633-8766 | Corporate.UDI@medtronic.com |
Regulatory Flags#
- DUNS number
- 006261481
- Device count
- 1
- Lot or batch
- true
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| 00643169508149 | SYNCHROMED® II | 8637-20 | 2016-04-27 | |
| 00643169508156 | SYNCHROMED® II | 8637-40 | 2016-04-27 | |
| 00643169630505 | SYNCHROMED® II | 8637-20 | 2018-08-17 | |
| 00643169630512 | SYNCHROMED® II | 8637-40 | 2018-08-17 | |
| 00643169100824 | SYNCHROMED ® II | 8637-40 | 2016-04-27 | |
| 00643169100831 | SYNCHROMED ® II | 8637-20 | 2016-04-27 | |
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