FlexCath Cross™ Transseptal Solution
- Primary DI
- 00763000925130
- Brand
- FlexCath Cross™ Transseptal Solution
- Company
- MEDTRONIC, INC.
- Model
- 900306
- Device description
- NDL 900306 FLEXCATH CROSS MH 63CM EIFU
- Published
- 2025-08-10
- Public version status
- New
- 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#
Product Code Classifications#
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K220047 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00763000925130 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00763000925130 | 00763000925130 | 763000925130 | 0763000925130 |
GMDN Terms#
| Term | Definition |
|---|---|
| Cardiac transseptal access electrosurgical dilator/needle | A luminal, one-piece, electrosurgical device designed to be used with a transseptal vascular guide-catheter (not included) to penetrate the interatrial septum for left-heart access during a transseptal catheterization procedure. It is typically a long, thin tube that is curved and round-nosed at the distal end for positioning against the atrial septum, and incorporates an extendable, sharp needle in its lumen able to apply radio-frequency (RF) alternating current in a monopolar configuration. It may have radiopaque markers for positioning and enable acquisition of an intracardiac electrocardiogram (ECG); a guidewire and connection cables may also be included. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | Keep dry |
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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| 00199150044191 | Concerto Versa™ | CVP-40 | 2026-10-18 | |
| 00199150044207 | Concerto Versa™ | CVP-65 | 2026-10-18 | |
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| 00824846020073 | NA | BB10E56R16 | 2026-10-01 | |
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| 00199150032426 | SenSight™ | B31030-D | 2026-09-28 | |
| 00763000923709 | Power Cord | MCS1621PC | 2026-09-25 | |
| 00763000443214 | NA | 2ACHC | 2024-05-18 | |
| 00763000368470 | Aurora EV-ICD™ MRI SureScan™ | DVEA3E4 | 2023-11-02 | |
| 00763000001513 | Primo MRI™ DR SureScan™ | DDMD3D4 | 2018-06-02 | |
| 00763000001551 | Primo MRI™ VR SureScan™ | DVMD3D4 | 2018-06-02 | |
| 00763000059491 | Evera MRI™ XT DR SureScan® | DDMB1D4 | 2017-10-20 | |
| 00763000059651 | Viva™ Quad XT CRT-D | DTBA1QQ | 2017-10-21 | |
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| 00763000059705 | Evera MRI™ S DR SureScan® | DDMC3D4 | 2017-10-21 | |
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