DEVICE: Frontier™ (05414734502948)
Device Identifier (DI) Information
Frontier™
II
Not in Commercial Distribution
5586
ST. JUDE MEDICAL, INC.
II
Not in Commercial Distribution
5586
ST. JUDE MEDICAL, INC.
Cardiac Resynchronization Therapy Pacemaker (CRT-P)
DDDRV
Device Characteristics
Labeling does not contain MRI Safety Information | |
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? |
---|---|---|---|---|
47263 | Cardiac resynchronization therapy implantable pacemaker |
A battery-powered, hermetically-sealed pulse generator, intended to be implanted beneath the skin of the chest in a surgically-created pocket, and used with pacing leads placed in the right ventricle, in a coronary vein over the left ventricle, and often in the right atrium (triple chamber) to stimulate the heart to beat at a faster rate when it senses bradycardia and provides cardiac resynchronization therapy (CRT) through biventricular electrical stimulation to synchronize right and left ventricular contractions to treat symptoms of heart failure (e.g., easy fatigue) and serious heart-rhythm problems [CRT pacemaker (CRT-P)]; it is not intended for defibrillation therapy.
|
Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
NKE | Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P) |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
P030035 | 001 |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Handling Environment Temperature: between 23 and 122 Degrees Fahrenheit |
Storage Environment Temperature: between -5 and 50 Degrees Celsius |
Handling Environment Temperature: between -5 and 50 Degrees Celsius |
Storage Environment Temperature: between 23 and 122 Degrees Fahrenheit |
Clinically Relevant Size
[?]Size Type Text |
---|
Total Volume: 11.5 Milliliter |
Device Record Status
a66324c8-6bc8-49e4-8913-b9d5693cb628
February 05, 2021
4
February 03, 2017
February 05, 2021
4
February 03, 2017
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(855)478-5833
customerservice@sjm.com
customerservice@sjm.com