DEVICE: EXCOR® (04260090040560)
Device Identifier (DI) Information
EXCOR®
L20H-002x01
In Commercial Distribution
Berlin Heart GmbH
L20H-002x01
In Commercial Distribution
Berlin Heart GmbH
Driving tube, red
Ø 6/8 mm L 2 m
Device Characteristics
| MR Unsafe | |
| No | |
| No | |
| Yes | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 10847 | External ventricular circulatory assist system |
An assembly of devices intended to assist a damaged or weakened heart (e.g., one affected by cardiogenic shock) to pump blood. It includes a electrically-powered external pump, an atrial or ventricular cannula to draw blood outside the body, a cannula to deliver the blood back to the aorta or pulmonary artery (depending on left or right ventricular assistance), and a unit that controls pump operation. It is typically intended to be used as a bridge to heart transplantation; it is not intended for cardiopulmonary bypass.
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| DSQ | Ventricular (Assisst) Bypass |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| H100004 | 003 |
| H100004 | 004 |
| H100004 | 006 |
| H100004 | 008 |
| H100004 | 011 |
| H100004 | 013 |
| H100004 | 017 |
| H100004 | 021 |
| P160035 | 000 |
| P160035 | 001 |
| P160035 | 011 |
| P160035 | 016 |
| P160035 | 019 |
| P160035 | 024 |
| P160035 | 037 |
| P160035 | 041 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Humidity: between 35 and 50 Percent (%) Relative Humidity |
| Storage Environment Temperature: between 15 and 25 Degrees Celsius |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Lumen/Inner Diameter: 6 Millimeter |
Device Record Status
817d7e4e-8c9f-4e69-b075-6df6e398ab43
August 20, 2024
9
September 24, 2014
August 20, 2024
9
September 24, 2014
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
1.281.863.9700
info@berlinheartinc.com
info@berlinheartinc.com