DEVICE: Fisher & Paykel Healthcare (09420012457653)
Device Identifier (DI) Information
Fisher & Paykel Healthcare
my820JUS
In Commercial Distribution
my820JUS
FISHER & PAYKEL HEALTHCARE LIMITED
my820JUS
In Commercial Distribution
my820JUS
FISHER & PAYKEL HEALTHCARE LIMITED
Respiratory Humidifier
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| No | |
| 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? |
|---|---|---|---|---|
| 57828 | Professional high-flow respiratory unit, humidifying, manual |
An electrically-powered device designed to deliver high-flow (exceeding peak inspiratory flow) heated and humidified ambient air or air/oxygen, at a manually set oxygen concentration (FiO2), to a spontaneously breathing patient. It is intended for use by a healthcare provider as part of noninvasive ventilation (NIV), in a peri-anaesthesia environment, or for a patient experiencing a respiratory disorder [e.g., chronic obstructive pulmonary disease (COPD)]. It typically consists of a gas flow generator, a heating element, and humidification chamber.
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Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| BTT | Humidifier, Respiratory Gas, (Direct Patient Interface) |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| K223684 | 000 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Storage Environment Temperature: between -25 and 70 Degrees Celsius |
| Storage Environment Humidity: between 10 and 95 Percent (%) Relative Humidity |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| No Device Sizes |
Device Record Status
2c0d9d3f-b566-4cf6-a330-bd4c63870701
May 08, 2024
1
April 30, 2024
May 08, 2024
1
April 30, 2024
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
[?]
1800 446 3908
Customer.CareUSA@fphcare.com
Customer.CareUSA@fphcare.com