Agilis™ NxT Steerable Introducer Dual-Reach™
- Primary DI
- 05415067051851
- Brand
- Agilis™ NxT Steerable Introducer Dual-Reach™
- Company
- ST. JUDE MEDICAL, INC.
- Model
- SI-1371-M
- Catalog number
- SI-1371-M
- Device description
- Steerable Introducer
- Published
- 2025-02-07
- 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
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| DYB | Introducer, catheter |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DYB | Introducer, Catheter | Cardiovascular | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K243493 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 05415067051851 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 05415067051851 | 05415067051851 | 5415067051851 |
GMDN Terms#
| Term | Definition |
|---|---|
| Vascular guide-catheter, single-use | A flexible tube intended to be used for the percutaneous transluminal passage and placement of a diagnostic/interventional catheter, lead (e.g., pacing lead, balloon dilatation catheter), needle or guidewire through its lumen(s), within the vascular system. It may be rigid or flexible, non-steerable or steerable, single or multiple lumen(s), and the distal section can have a variety of preformed shapes. It is not intended solely for infusion nor to access superselective small vessels, and does not include a transseptal needle. A percutaneous introduction set, shaft visualization electrodes, or haemostatic valve may be supplied with the guide-catheter. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 0 | |
| Length | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Excursions permitted from -20°C to 50°C, and 10%-90% store at room temperature 10°C to 25°C, Keep dry, keep away from sunlight, protect from heat and radioactive sources |
Contacts#
| Phone | |
|---|---|
| +1(855)478-5833 | customerservice@sjm.com |
Regulatory Flags#
- DUNS number
- 149818952
- 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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| 05415067032195 | EnSite™ | ENSITE-FF-01 | ENSITE-FF-01 | 2021-01-06 |
| 05415067032201 | EnSite™ | ENSITE-R-FF-01 | ENSITE-R-FF-01 | 2021-01-06 |
| 05415067024732 | EnSite Precision™ | H702473 | H702473 | 2020-07-22 |
| 05415067024695 | EnSite Precision™ | H702469 | H702469 | 2016-12-20 |
| 05415067024701 | EnSite Precision™ | H702470 | H702470 | 2016-12-20 |
| 05415067024756 | EnSite Precision™ Link, Sensor Enabled™ | H702475 | H702475 | 2016-12-20 |
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| 05415067055668 | EnSite™ | ENSITE-D-PI-01 | ENSITE-D-PI-01 | 2026-08-19 |
| 05415067055675 | EnSite™ | ENSITE-PI-01 | ENSITE-PI-01 | 2026-08-19 |
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