Amplatzer™ Talisman™
- Primary DI
- 05415067033307
- Brand
- Amplatzer™ Talisman™
- Company
- ST. JUDE MEDICAL, INC.
- Model
- 9-PFO-1818
- Catalog number
- 9-PFO-1818
- Device description
- PFO Occluder
- Published
- 2021-09-29
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| MLV | Transcatheter septal occluder |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| MLV | Transcatheter Septal Occluder | Unknown | 3 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 05415067033307 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 05415067033307 | 05415067033307 | 5415067033307 |
GMDN Terms
| Term | Definition |
|---|---|
| Cardiac occluder | An implantable disk-like device intended to be used for the minimally-invasive closure of cardiac defects and deployed using a dedicated delivery catheter/sheath. It is made of wire mesh [e.g., nickel-titanium alloy (Nitinol)], and possibly additional materials (e.g., polyester), and is typically self-expandable. The device is used to treat cardiac disorders that may include (but not limited to) atrial septal defect (ASD), ventricular septal defect (VSD), patent foramen ovale (PFO), or patent ductus arteriosus (PDA). Disposable devices dedicated to implantation may be included with the implant. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Catheter Gauge | 8 | French |
| Outer Diameter | 18 | Millimeter |
Sterilization Methods
| Method |
|---|
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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Other Devices Sharing Product Codes
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 05415067033314 | Amplatzer™ Talisman™ | ST. JUDE MEDICAL, INC. | MLV | 2021-09-29 |
| 05415067033321 | Amplatzer™ Talisman™ | ST. JUDE MEDICAL, INC. | MLV | 2021-09-29 |
| 05415067033345 | Amplatzer™ Talisman™ | ST. JUDE MEDICAL, INC. | MLV | 2021-09-29 |
| 00733132636525 | GORE CARDIOFORM ASD Occluder | W. L. Gore & Associates, Inc. | MLV | 2019-08-07 |
| 00733132636488 | GORE CARDIOFORM ASD Occluder | W. L. Gore & Associates, Inc. | MLV | 2019-07-03 |
| 00733132636495 | GORE CARDIOFORM ASD Occluder | W. L. Gore & Associates, Inc. | MLV | 2019-07-03 |
| 00733132636501 | GORE CARDIOFORM ASD Occluder | W. L. Gore & Associates, Inc. | MLV | 2019-07-03 |
| 00733132636518 | GORE CARDIOFORM ASD Occluder | W. L. Gore & Associates, Inc. | MLV | 2019-07-03 |
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| H373HX202534 | GORE HELEX Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| H373HX203030 | GORE HELEX Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| H373HX203535 | GORE HELEX Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| 00733132617609 | Gore Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| 00733132631001 | GORE CARDIOFORM Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| 00733132631018 | GORE CARDIOFORM Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| 00733132631025 | GORE CARDIOFORM Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
| 00733132631032 | GORE CARDIOFORM Septal Occluder | W. L. Gore & Associates, Inc. | MLV | 2017-02-13 |
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| 00811806011288 | Amplatzer™ | ST. JUDE MEDICAL, INC. | MLV | 2016-11-08 |
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